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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427295Generated: November 2, 2026

Sodium Thiosulfate → Ethyl 1-formylcyclopropanecarboxylate

https://huagongshe.com/reaction/2427295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium BromideHCID 253881—
ReactantSodium BicarbonateHCID 516892—
ReactantTempoHCID 2724126—
ReactantEthyl 1-(hydroxymethyl)cyclopropane-1-carboxylateHCID 12450336—
ReactantSodium HypochloriteHCID 23665760—
SolventDichloromethaneHCID 6344—
ProductEthyl 1-formylcyclopropanecarboxylateHCID 9964122100.5%

Reaction Steps

To a solution of Preparation 232 1-hydroxymethyl-cyclopropanecarboxylic acid ethyl ester (3.00 g, 21.00 mmol) in dichloromethane (50 ml), at 0° C., was added saturated sodium hydrogen carbonate solution (50 ml), followed by TEMPO (659 mg, 4.00 mmol) and sodium bromide (400 mg, 4.00 mmol). After stirring for 5 min, sodium hypochlorite solution (10%, 14.00 mmol) was added slowly, followed by saturated sodium thiosulphate solution (50 ml). The two layers were separated and the aqueous layer was extracted with dichloromethane. The combined organic phases were dried (MgSO4) and concentrated in vacuo to give the titled compound (3.00 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968584B2
Source datasetuspto-grants-2011_06
ORD IDord-224830ab8ab94940bce5bae8a8a6c906
Source noteuspto-grants-2011_06