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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1715083Generated: October 30, 2026

HCID 57792846, compound → HCID 58208601, compound

https://huagongshe.com/reaction/1715083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57792846HCID 57792846—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 58208601HCID 58208601—

Reaction Conditions

Temperature20 °C

Reaction Steps

Preparation of (3R,3aR,6S,6aS)-Benzyl 3-hydroxy-6-(tosyloxy)tetrahydro-2H-furo[3,2-b]pyrrole-4(5H)-carboxylate (34). Ethanol (6 mL) was added dropwise to a mixture of 10% palladium on charcoal (50 mg) and anti-(33) (547 mg, 1.26 mmol) under an atmosphere of argon. The argon was replaced by hydrogen then the suspension was stirred at 20° C. for 3.75 hours before filtering the mixture through celite in vacuo. The filter cake was washed with ethanol (40 mL) then the solvents removed in vacuo from the filtrate to obtain (3R,3aR,6S,6aS)-3-hydroxyhexahydro-2H-furo[3,2-b]pyrrol-6-yl 4-methylbenzenesulfonate which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799791B2
Source datasetuspto-grants-2010_09
ORD IDord-0a979ca2179047e2849497be837f6094
Source noteuspto-grants-2010_09