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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602580Generated: October 25, 2026

Benzyl Alcohol → (2RS,3SR)-2-benzyloxycarbonyl-5-oxotetrahydrofuran-3-carboxylic acid

https://huagongshe.com/reaction/1602580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantTetrahydro-5-oxofuran-2,3-dicarboxylic acidHCID 98259—
SolventAcetoneHCID 180—
Product(2RS,3SR)-2-benzyloxycarbonyl-5-oxotetrahydrofuran-3-carboxylic acidHCID 18705291—

Reaction Steps

5.2 g of (2RS,3SR)-5-oxotetrahydrofuran-2,3-dicarboxylic acid in 88 ml of acetone was stirred together with 6.5 g of 1,1'-dicyclohexylcarbodiimide at room temperature for 2 hours. After addition of 3.26 ml of benzyl alcohol, the reaction solution was stirred at the same temperature for 12 hours. The insolubles were filtered off, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography [hexane/ethyl acetate=4/1→chloroform/methanol=50/1] to give 7.93 g of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981573
Source datasetuspto-grants-1999_11
ORD IDord-7855acd2cfb64c55b9059c98b3a8d799
Source noteuspto-grants-1999_11