HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212452Generated: October 26, 2026
Acetyl chloride → Cyclohexyl (S)-3-(3,4-dihydroxyphenyl)-2-hydrazino-2-methylpropanoate
https://huagongshe.com/reaction/2212452
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Reactant | Carbidopa | HCID 34359 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Cyclohexyl (S)-3-(3,4-dihydroxyphenyl)-2-hydrazino-2-methylpropanoate | HCID 86594119 | — |
Reaction Steps
Acetyl chloride (1 mL) was slowly added to cyclohexanol (5 mL) at 0° C. After stirring at 0° C. for 10 min, carbidopa (294 mg, 1.5 mmol) was added slowly as solid. The resulting mixture was warmed to 50° C. for 16 h. After cooling to room temperature, ethyl acetate (40 mL) was added and product was extracted with water (4×5 mL), then the aqueous phase was lyophilized to give the crude product. HPLC of the crude product afforded 50 mg of the title compound as an oil. 1H NMR (CD3OD): δ 1.46 (s, 3H), 1.52–1.80 (m, 10H), 2.92 (dd, J=13.6 Hz, 2H,), 4.85 (m, 1H), 6.49 (d, J=7.6 Hz, 1H), 6.59 (s, 1H), 6.68 (d, J=7.6 Hz, 1H). MS (ESI) m/z 309.3 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07101912B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-e04c3f88f0e341cf98c9e0671be78b4f |
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| Source note | uspto-grants-2006_09 |
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