HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67278Generated: October 26, 2026
Hydrochloric Acid → 4-Dichloromethyl-6,6-dimethyl-3-oxabicyclo[3.1.0]hexan-2-one
https://huagongshe.com/reaction/67278
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | cis 2-(1-Hydroxy-2,2,2-trichloroethyl)-3,3-dimethycyclopropane carboxylic acid | HCID 86738542 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Dichloromethyl-6,6-dimethyl-3-oxabicyclo[3.1.0]hexan-2-one | HCID 20492984 | 25% |
Reaction Steps
Sodium borohydride (0.12 mmol) was added to a solution of cis 2-(1-hydroxy-2,2,2-trichloroethyl)-3,3-dimethylcyclopropane carboxylic acid (0.12 mol) in dry dimethylformamide (0.4 ml), and the mixture was heated for 30 minutes at 80° C. An additional amount of 0.12 mmol sodium borohydride was then added and the mixture was heated for a further 15 minutes at 80° C. It was then diluted with water, acidified with concentrated HCl and extracted with deuterochloroform, CDCl3. The extract was washed with water and analysed by NMR, which showed a yield of 25% of the desired product, with 30% of unconverted starting material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04346038 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-1172febbe3854caaae15a576756d9404 |
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| Source note | uspto-grants-1982_08 |
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