聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 3-氨甲基苯甲醇

A solution of 3-(hydroxymethyl)benzonitrile in THF was slowly added to a refluxing solution of LiAlH4 in THF with vigorous stirring, maintained under nitrogen atmosphere. The solution was heated at reflux overnight and water was thereafter slowly added dropwise to quench the reaction (until no further evolution of H2 was apparent). The THF was evaporated under reduced pressure and ether/acidified water was added. The ether phase was discarded. The aqueous phase was washed with ether and the organic phase was discarded. NaOH was added until the pH of the aqueous phase reached pH 7. The solution was extracted with THF three times, dried over MgSO4 and evaporated under reduced pressure to furnish a slightly yellow residue which was purified by chromatography on a silica gel column using a gradient eluent starting from ethyl acetate and ending with a mixture of 1:1 ethyl acetate:MeOH), to give the intermediate in a 40% yield.

1. temperaturemaintained under nitrogen atmosphere
2. temperatureThe solution was heated
3. temperatureat reflux overnight
4. customto quench
5. customthe reaction (until no further evolution of H2
6. customThe THF was evaporated under reduced pressure and ether/
7. additionwas added
8. washThe aqueous phase was washed with ether
9. additionNaOH was added until the pH of the aqueous phase
10. extractionThe solution was extracted with THF three times
11. dry with materialdried over MgSO4
12. customevaporated under reduced pressure
13. customto furnish a slightly yellow residue which
14. customwas purified by chromatography on a silica gel column
15. additionending with a mixture of 1:1 ethyl acetate
16. customMeOH), to give the intermediate in a 40% yield

ORD记录

ord-975406b824224c50944eb6894d13a310

来源数据集

uspto-grants-2012_01

DOI

10.6084/m9.figshare.5104873.v1

专利号

US08088941B2