Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1072886Generated: November 1, 2026

Water → 2-Chloro-4-(n-pentyl)benzyl alcohol

https://huagongshe.com/reaction/1072886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTBAF tetrahydrofuranHCID 11078149—
Reactant1-((tert-Butyldiphenylsilyloxy)methyl)-2-chloro-4-(n-pentyl)benzeneHCID 22388382—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-4-(n-pentyl)benzyl alcoholHCID 5369947382.2%

Reaction Steps

A solution (1.0 M, 2.4 ml) of tetrabutylammonium fluoride/tetrahydrofuran was added to a solution of 1-((tert-butyldiphenylsilyloxy)methyl)-2-chloro-4-(n-pentyl)benzene (890 mg) in tetrahydrofuran (4.5 ml) under ice-cooling, and the mixture was stirred for 2 hr. Water was added to the reaction mixture and the resulting product was extracted three times with ethyl acetate. The organic layers were combined and washed successively with diluted hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=7/1) to give the objective compound (345 mg) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06911469B2
Source datasetuspto-grants-2005_06
ORD IDord-d4ae530da7514597bccb88800af7f1de
Source noteuspto-grants-2005_06