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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl dichloroacetate | HCID 8315 | — |
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-tert-butoxycarbonyl-1-chloro-1-cyclopropanecarboxylate | HCID 10014285 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05780669 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-acfe2c0dd7c04502ac76248e379b1f73 |
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| Source note | uspto-grants-1998_07 |
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