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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956826Generated: October 25, 2026

Hydrochloric Acid → Methyl 2-tert-butoxycarbonyl-1-chloro-1-cyclopropanecarboxylate

https://huagongshe.com/reaction/1956826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl dichloroacetateHCID 8315—
Reactanttert-Butyl acrylateHCID 15458—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-tert-butoxycarbonyl-1-chloro-1-cyclopropanecarboxylateHCID 1001428584%

Reaction Conditions

Temperature10 °C

Reaction Steps

80 g of 60% sodium hydride was suspended in 1,000 ml of N,N-dimethylformamide. To this suspension was dropped 352 ml of tert-butyl acrylate within 30 minutes under ice-cooling. Then 207 ml of methyl dichloroacetate was dropped into this reaction mixture within 1.5 hours while maintaining the internal temperature at 10° C. After the completion of the addition, the mixture was stirred for 2 hours while maintaining the internal temperature at 10° to 20° C. Then the reaction mixture was neutralized by adding concentrated hydrochloric acid and water was-further added thereto. The reaction mixture was extracted with ethyl acetate and the organic layer was washed with a saturated aqueous solution of sodium chloride. The extract was dried over anhydrous sodium sulfate and then the solvent was evaporated under reduced pressure. The obtained residue was distilled under reduced pressure to thereby give 384 g (yield 84%) of methyl 2-tert-butoxycarbonyl-1-chloro-1-cyclopropanecarboxylate in the form of a colorless oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780669
Source datasetuspto-grants-1998_07
ORD IDord-acfe2c0dd7c04502ac76248e379b1f73
Source noteuspto-grants-1998_07