The present invention relates to a novel process for the synthesis of 9,9-bis(methoxymethyl)fluorene. The syntheses from fluorene to 9,9-bis(hydroxymethyl)fluorene via a hydroxymethylation and further to 9,9-bis(methoxymethyl)fluorene via a etherification are known. 9,9-bis(methoxymethyl)fluorene is a compound that is used as an electron donor for Ziegler-Natta catalysts. The present invention is related to an improvement in the synthesis of 9,9-bis(methoxymethyl)fluorene leading to a decrease in the amount of solvent used and an easier work up while achieving high yield and purity.

The present invention relates to a novel process for the synthesis of 9,9-bis(methoxymethyl)fluorene. The syntheses from fluorene to 9,9-bis(hydroxymethyl)fluorene via a hydroxymethylation and further to 9,9-bis(methoxymethyl)fluorene via a etherification are known. 9,9-bis(methoxymethyl)fluorene is a compound that is used as an electron donor for Ziegler-Natta catalysts. The present invention is related to an improvement in the synthesis of 9,9-bis(methoxymethyl)fluorene leading to a decrease in the amount of solvent used and an easier work up while achieving high yield and purity.

The present invention relates to a novel process for the synthesis of 9,9-bis(methoxymethyl)fluorene. The syntheses from fluorene to 9,9-bis(hydroxymethyl)fluorene via a hydroxymethylation and further to 9,9-bis(methoxymethyl)fluorene via a etherification are known. 9,9-bis(methoxymethyl)fluorene is a compound that is used as an electron donor for Ziegler-Natta catalysts. The present invention is related to an improvement in the synthesis of 9,9-bis(methoxymethyl)fluorene leading to a decrease in the amount of solvent used and an easier work up while achieving high yield and purity.

The present invention relates to the field of malodor counteraction. More particularly, it concerns malodor masking ingredient having an indane moiety (as defined in formula (I)), as well as malodor masking compositions comprising such ingredients.

The present invention relates to the field of malodor counteraction. More particularly, it concerns malodor masking ingredient having an indane moiety (as defined in formula (I)), as well as malodor masking compositions comprising such ingredients.

A liquid crystal composition includes a first compound expressed by Chemical Formula I,

##STR00001##

In Chemical Formula

##STR00002##

is at least one of a cyclohexyl group and phenyl group,

##STR00003##

is at least one of a cyclohexyl group and a phenyl group, each of n and m is a natural number of 1 to 4, n+m is 2 to 5, and R is at least one of a C.sub.1-10 alkyl group, a C.sub.2-10 alkenyl group, and a C.sub.1-10 alkoxy group.

A liquid crystal composition includes a first compound expressed by Chemical Formula I,

##STR00001##

In Chemical Formula

##STR00002##

is at least one of a cyclohexyl group and phenyl group,

##STR00003##

is at least one of a cyclohexyl group and a phenyl group, each of n and m is a natural number of 1 to 4, n+m is 2 to 5, and R is at least one of a C.sub.1-10 alkyl group, a C.sub.2-10 alkenyl group, and a C.sub.1-10 alkoxy group.

Described herein are compounds of formula (I) as properfume compounds. In particular, described herein is a method to release a compound being a ketone of formula (II), a formate ester of formula (III), and/or an alcohol of formula (IV) by exposing the compound of formula (I) to an environment wherein it is oxidized. Moreover, a perfuming composition and a perfumed consumer product including at least one compound of formula (I) are also described.

Described herein are compounds of formula (I) as properfume compounds. In particular, described herein is a method to release a compound being a ketone of formula (II), a formate ester of formula (III), and/or an alcohol of formula (IV) by exposing the compound of formula (I) to an environment wherein it is oxidized. Moreover, a perfuming composition and a perfumed consumer product including at least one compound of formula (I) are also described.

Described herein are compounds of formula (I) as properfume compounds. In particular, described herein is a method to release a compound being a ketone of formula (II), a formate ester of formula (III), and/or an alcohol of formula (IV) by exposing the compound of formula (I) to an environment wherein it is oxidized. Moreover, a perfuming composition and a perfumed consumer product including at least one compound of formula (I) are also described.