HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528701Generated: October 30, 2026
Isopropenyl acetate → HCID 178501043, compound
https://huagongshe.com/reaction/528701
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropenyl acetate | HCID 7916 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178501086 | HCID 178501086 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178501043 | HCID 178501043 | 50% |
Reaction Steps
To a solution of trans-methyl 4-(chloro(hydroxyimino)methyl)cyclohexanecarboxylate (5.90 g, 26.9 mmol) and isopropenyl acetate (53.8 g, 537 mmol) in dichloromethane (134 ml) was added triethylamine (5.44 g, 53.7 mmol) at 0-5° C. The cooling bath was removed 15 minutes after completed addition, and the mixture was stirred for 20 h. The reaction mixture was concentrated in vacuo. The residue was partitioned between ethyl acetate (250 ml) and 0.1 M aqueous hydrochloric acid solution (200 ml). The organic layer was washed with one 100 ml-portion of 0.1 M aqueous hydrochloric acid solution. The combined aqueous layers were extracted with one 150 ml-portion of ethyl acetate. The combined organic layers were washed with one 200 ml-portion of 2 M sodium carbonate and one 100-ml portion of brine, dried over anhydrous sodium sulfate and concentrated in vacuo. Purification with n-heptane/ethyl acetate as eluent gave the title compound (3.00 g, 50%) as off-white solid. MS m/e: 224 ([M+H]+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346824B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-d47950ba2ae84e68899523a3e414dc8e |
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| Source note | uspto-grants-2016_05 |
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