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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6432Generated: October 28, 2026

Benzyl chloroformate → Methyl N-benzyloxycarbonyl-3,5-di-O-benzyl-2,6-dideoxy-2,6-imino-L-gulofuranoside

https://huagongshe.com/reaction/6432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 3,5-di-O-benzyl-2,6-dideoxy-2,6-imino-L-gulofuranosideHCID 54038294—
SolventDiethyl EtherHCID 3283—
ProductMethyl N-benzyloxycarbonyl-3,5-di-O-benzyl-2,6-dideoxy-2,6-imino-L-gulofuranosideHCID 11145393—

Reaction Steps

To the crude amine (15), in a solution of diethyl ether:saturated sodium bicarbonate (3:2, 20 ml), was added benzylchloroformate (0.2 ml, 1.2 mmol). The reaction was then stirred, at such a rate as to make it one phase, for 2 hours. The aqueous phase was then separated and washed with diethyl ether (3×10 ml). The combined ethereal layers were then dried (sodium sulphate) and the solvent removed in vacuo. Purification by flash chromatography (0-50%, diethyl ether/hexane) then yielded methyl N-benzyloxycarbonyl-3,5-di-O-benzyl-2,6-deoxy-2,6-imino-L-gulofuranoside (16), as a colorless oil (200 mg, 67% from azidotriflate). νmax (CHCl3): 1685, 750, 700 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248779
Source datasetuspto-grants-1993_09
ORD IDord-7c1e2ef533ec401fb17ad35bd72360ba
Source noteuspto-grants-1993_09