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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20911Generated: October 26, 2026

Sucrose → 1-(6-Benzyloxycarbonylamino-hexanoyl)-4-hydroxy-pyrrolidine-3-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/20911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSucroseHCID 5988—
Reactant1-(6-Benzyloxycarbonylamino-hexanoyl)-4-oxo-pyrrolidine-3-carboxylic Acid Ethyl EsterHCID 68637397—
SolventWaterHCID 962—
Product1-(6-Benzyloxycarbonylamino-hexanoyl)-4-hydroxy-pyrrolidine-3-carboxylic Acid Ethyl EsterHCID 6863747042.3%

Reaction Conditions

Temperature32 °C

Reaction Steps

To a solution of sucrose (3 g) in distilled water (40 mL) was added Baker's yeast (2 g). The suspension was heated at 32° C. for 1 h. The content of the flask was then poured into a flask containing ketoester 60 (4 g, 9.88 mmol, dissolved in 4 mL of methanol). Stirring was continued at 32° C. for 24 h after which additional sucrose (3 g) in warm (40° C.) distilled water was added. After 48 h, the suspension was filtered through a pad of Celite. The pad was washed with water and the aqueous layer was extracted with ethyl acetate (3×250 mL). The combined organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was subjected to flash chromatography (30% EtOAc/Hexane) to afford alcohol 62 (1.7 g, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745608B2
Source datasetuspto-grants-2010_06
ORD IDord-ca498f94fc9a49b0b286e48dce221305
Source noteuspto-grants-2010_06