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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891660Generated: October 30, 2026

Triethylamine → HCID 69583502, compound

https://huagongshe.com/reaction/891660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant(2S,3S)-2-Amino-3-methyl-1-pentanolHCID 2724027—
SolventDichloromethaneHCID 6344—
ProductHCID 69583502HCID 6958350288.3%

Reaction Steps

To a solution of L-isoleucinol (2.20 g, 18.8 mmol) in methylene chloride (66 ml) were added chloroformic acid benzyl ester (3.22 ml, 22.5 mmol) and triethylamine (3.15 ml, 22.5 mmol) in an ice bath, and the mixture was stirred at room temperature for 1.5 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate solution. The obtained organic layer was washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (2:1→1:1) as the eluant to afford [(1S,2S)-1-(hydroxymethyl)-2-methylbutyl]carbamic acid benzyl ester (4.17 g, yield 88%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001897B2
Source datasetuspto-grants-2006_02
ORD IDord-d033ff1f08b6420ea5772bc24c654e8c
Source noteuspto-grants-2006_02