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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660111Generated: October 27, 2026

Sulfuric Acid → 2-(N-Carbobenzyloxyglycylamino)-2-deoxy-D-glucitol

https://huagongshe.com/reaction/1660111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantBenzyloxycarbonylglycineHCID 14349—
ReactantGlucosaminitolHCID 189022—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Solvent1,4-DioxaneHCID 31275—
SolventBenzene methyl ketoneHCID 22015841—
Product2-(N-Carbobenzyloxyglycylamino)-2-deoxy-D-glucitolHCID 70567425—

Reaction Steps

A mixture of 275 ml. of dry tetrahydrofuran and 275 ml. of dry dioxane was cooled to -5° and 12.88 ml. (9.35 g., 0.092 mole) of triethylamine, 8.74 ml. (9.96 g., 0.092 mole) of ethyl chloroformate and 19.23 g. (0.092 mole) of N-carbobenzyloxyglycine were added. The mixture was stirred for 15 min. at -5° and then a cold (0°-5°) solution of 16.65 g. (0.092 mole) of 2-amino-2-deoxy-D-glucitol in 40 ml. of water was added in one portion. The cooling bath was removed and the mixture was allowed to stir at ambient temperature for four hours. The solvent was evaporated in vacuum at 30°-40° and the residue was stirred overnight with 500 ml. of ethanol. Filtration furnished 30 g. of a solid. The solid was recrystallized from 700 ml. of methanol to give 21 g. of product. Tlc shows the product to be pure (silica gel plate--benzene/methyl ketone/88% formic acid 60:25:25--methanolic sulfuric acid development).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04307072
Source datasetuspto-grants-1981_12
ORD IDord-4e75e23cfe214b278b145b1725430a1f
Source noteuspto-grants-1981_12