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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111757Generated: November 3, 2026

Cyclopropanecarbonyl chloride → tert-Butyl cyclopropanecarboxylate

https://huagongshe.com/reaction/2111757

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiethyl EtherHCID 3283—
Producttert-Butyl cyclopropanecarboxylateHCID 13676038—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of 12.0 g (107.1 mmol) of potassium t-butoxide in 200 mL ether at 0° C. under nitrogen was added 13.4 g (128.6 mmol) of cyclopropanecarboxylic acid chloride over 5 min. After 30 min at 0° C. the mixture was stirred at ambient temperature for an additional 30 min. The reaction mixture was poured into aqueous saturated sodium bicarbonate and extracted with ether. The organic layer was dried and carefully concentrated to deliver 15.0 g (99%) of a yellow oil as the desired ester product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07521445B2
Source datasetuspto-grants-2009_04
ORD IDord-873c2b89f48e4ee7a6af8cf435b72baa
Source noteuspto-grants-2009_04