Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375760Generated: November 1, 2026

tert-Butanol → HCID 69212984, compound

https://huagongshe.com/reaction/2375760

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 22994173HCID 22994173—
SolventChloroformHCID 6212—
ProductHCID 69212984HCID 6921298426.5%

Reaction Conditions

Temperature-30 °C

Reaction Steps

A solution of 3 g (9.1 mmol) of 4-[2-[[(phenylmethoxy)carbonyl]amino]-ethoxy]benzeneacetic acid in 60 ml of chloroform is cooled to −30° C. and 1.18 g (10.9 mmol) of ethyl chloroformate and 1.52 ml (10.9 mmol) of triethylamine are added. The mixture is stirred for 1 hour at −30° C. and 1.63 g (22 mmol) of t-butanol and 1.52 ml (10.9 mmol) of triethylamine are then added. The mixture is stirred for 16 hours at room temperature and then concentrated under reduced pressure. The evaporation residue is taken up in 100 ml of ethyl acetate and the organic phase obtained is washed with water and then dried over magnesium sulfate and concentrated under reduced pressure. The crude product is purified by chromatography on silica gel using a dichloromethane/methylcyclohexane mixture (1/1; v/v) as the eluent to give 930 mg of the expected compound (yield=26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465811B2
Source datasetuspto-grants-2008_12
ORD IDord-6df0c8e71a414521a45cc43be3f3165b
Source noteuspto-grants-2008_12