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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082978Generated: October 25, 2026

L-Isoleucine → tert-Butoxycarbonyl-L-isoleucine

https://huagongshe.com/reaction/2082978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-IsoleucineHCID 6306—
ReactantTriethylamineHCID 8471—
Reactant1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazoleHCID 13292852—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Producttert-Butoxycarbonyl-L-isoleucineHCID 2724762104.7%

Reaction Steps

A suspension of 1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazole (2.7 g.), L-isoleucine (1.3 g) and triethylamine (3.5 ml.) in a mixture of water (8 ml.) and tert-butyl alcohol (12 ml.) was stirred for 2 hours at 60° to 62° C. tert-Butyl alcohol was distilled off from the reaction mixture under reduced pressure and water (15 ml.) was added to the residue. The mixture was adjusted to pH 3 with a citric acid aqueous solution under ice-cooling and extracted with ethyl acetate. The extract was then washed with water and a saturated sodium chloride aqueous solution. The thus formed precipitates were filtered off and then the filtrate was dried over magnesium sulfate. The solution was concentrated and a mixture of ether and petroleum ether (1:1) was added to the residue. An insoluble material was filtered off and the filtrate was concentrated under reduced pressure to give N-tert-butoxycarbonyl-L-isoleucine (2.4 g.), oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04083848
Source datasetuspto-grants-1978_04
ORD IDord-b22ab13b38ca4eb3b2dc85c02d6e6e27
Source noteuspto-grants-1978_04