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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235198Generated: November 1, 2026

Benzyl Alcohol → (1-Phenyl-cyclohexyl)-carbamic acid benzyl ester

https://huagongshe.com/reaction/2235198

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTriethylamineHCID 8471—
Reactant1-Phenylcyclohexane-1-carboxylic acidHCID 70817—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
SolventBenzeneHCID 241—
Product(1-Phenyl-cyclohexyl)-carbamic acid benzyl esterHCID 5929931638%

Reaction Conditions

Temperature80 °C

Reaction Steps

Dissolve 1-phenyl-cyclohexanecarboxylic acid (5.0 g, 24.48 mmol) in benzene (200 mL). Add triethylamine (2.45 g, 24.48 mmol), diphenylphosphoryl azide (6.74 g, 24.48 mmol), and benzyl alcohol (3.97 g, 36.72 mmol) under nitrogen. Stir and heat the reaction mixture to 80° C. Continue to heat the reaction at 80° C. for 8 hours, then cool to room temperature. Add water (250 mL), and extract the aqueous layer with ethyl acetate (3×300 mL). Combine the organic layers and dry with Na2SO4, filter, concentrate and purify by flash column chromatography (silica gel, 5-25% of EtOAc/Hexane) to give 2.87 g (38%) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713979B2
Source datasetuspto-grants-2010_05
ORD IDord-2fbe188cdd314f84b899a53aec685cf6
Source noteuspto-grants-2010_05