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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165077Generated: October 31, 2026

Acetone → 4-Ethoxycarbonyl-1,2-cyclopentanediol

https://huagongshe.com/reaction/1165077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
ReactantMethyl morpholine oxideHCID 82029—
ReactantEthyl 3-Cyclopentene-1-carboxylateHCID 5314991—
ReactantSodium BisulfiteHCID 23665763—
CatalystOsmium TetroxideHCID 30318—
SolventEthyl acetate hexaneHCID 21226206—
Product4-Ethoxycarbonyl-1,2-cyclopentanediolHCID 14476147—

Reaction Steps

A solution containing 84.6 g of N-methylmorpholine N-oxide, 1 g of osmium tetroxide, 230 ml of water and 115 ml of acetone was allowed to stir for 30 minutes at room temperature. To this stirred mixture was added, very slowly over at least 8 hours, a solution of 80 g of ethyl 3-cyclopentene-1-carboxylate in 115 ml of acetone. The stirred mixture was heated at 50° C. for 2 hours to complete the reaction (verified by TLC examination using ethyl acetate/hexane 70/30). Sodium bisulfite (~10 g) was added, the stirring continued for a further 15 minutes, and the mixture filtered through Celite. The pH of the filtrate was adjusted to 7 by the addition of 12 N sulfuric acid (37 ml), the acetone evaporated, the pH of the residual solution adjusted to 2 with 12 N sulfuric acid (13 ml) and the solution extracted with ethyl acetate (4×250 ml). Evaporation of the dried ethyl acetate solution gave 4-ethoxycarbonyl-1,2-cyclopentanediol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906755
Source datasetuspto-grants-1990_03
ORD IDord-684e9ce17e94439d971a4498b89c7da3
Source noteuspto-grants-1990_03