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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 255617Generated: November 1, 2026

Methanol → Methyl (2S,3S)-3-t-butoxycarbonylamino-2-hydroxy-5-methylhexanoate

https://huagongshe.com/reaction/255617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDiazomethaneHCID 9550—
Reactant(2RS,3S)-3-tert-butyloxycarbonylamino-2-hydroxy-5-methylhexanoic acidHCID 13848631—
SolventDiethyl EtherHCID 3283—
ProductMethyl (2S,3S)-3-t-butoxycarbonylamino-2-hydroxy-5-methylhexanoateHCID 13420965—

Reaction Steps

A solution of 1.00 g (3.8 mmole) of 3(S)-t-butoxycarbonylamino-2-hydroxy-5-methylhexanoic acid prepared by the method of R. L. Johnson [J. Med. Chem., 25, 605 (1982)] in 30 ml, of methanol was stirred, whilst cooling with ice, and then a diethyl ether solution of diazomethane was added and the mixture was stirred at room temperature for 1 hour. The solvent was then distilled off and the resulting solid was recrystallized from hexane to give 952 mg of the title product as colorless needles, melting at 84°-85° C.; [α]25 -10.2° (C=1.26, methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04698329
Source datasetuspto-grants-1987_10
ORD IDord-f1602008bb59499aa40402308358b05b
Source noteuspto-grants-1987_10