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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020378Generated: October 26, 2026

Ethyl 2-formylcyclopropanecarboxylate → Ethyl 2-(hydroxymethyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1020378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-formylcyclopropanecarboxylateHCID 89334—
ReactantSodium borohydrideHCID 4311764—
SolventEthanolHCID 702—
ProductEthyl 2-(hydroxymethyl)cyclopropanecarboxylateHCID 1300570768%

Reaction Steps

To a solution of ethyl 2-formylcyclopropanecarboxylate (2.00 g, 13.68 mmol) in absolute ethanol (55.0 mL) at room temperature and under an anhydrous atmosphere was added sodium borohydride (0.776 g, 20.53 mmol) in one portion. The reaction mixture was stirred at room temperature for 5 h then quenched with an aqueous pH 7 phosphate buffer solution (100 mL) and the ethanol was removed under reduced pressure. The aqueous layer was mixed with methylene chloride (100 mL), decanted, then extracted with methylene chloride (2×100 mL). The combined organic extracts were then successively washed with an aqueous pH 7 phosphate buffer solution (70 mL) and brine (70 mL), dried over MgSO4, filtered, and concentrated to give ethyl 2-(hydroxymethyl)cyclopropanecarboxylate (C-5) as a light yellow oil (1.334 g, 68% yield), which was used for the next step without additional purification. MS (M+1): m/e 145.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716312B2
Source datasetuspto-grants-2014_05
ORD IDord-d062a491fd814eda9ed076f0ae077e43
Source noteuspto-grants-2014_05