HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235224Generated: November 1, 2026
Water → 4-chloro-N-(1-methylcyclohexyl)butanamide
https://huagongshe.com/reaction/2235224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | 1-Amino-1-methylcyclohexane | HCID 3021578 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-chloro-N-(1-methylcyclohexyl)butanamide | HCID 63308335 | 90% |
Reaction Steps
Dissolve 1-methylcyclohexanamine (0.78 g, 6.89 mmol) in anhydrous THF (100 mL) and cool to 0° C. Add Et3N (3.49 g, 34.45 mmol) and 4-chlorobutanoyl chloride (1.94 g, 13.78 mmol) with stirring under N2. Stir the reaction mixture for 2 hours at room temperature and add water (100 mL). Extract the aqueous with EtOAc (3×200 mL) and then combine the organic layers and dry with Na2SO4, filter, concentrate and purify by flash column chromatography (silica gel, 30-80% of EtOAc-Hexane) to give 1.35 g (90%) of 4-chloro-N-(1-methylcyclohexyl)butanamide as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07713979B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-8052b365b29d47b8bcb3b3fa9ceb8112 |
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| Source note | uspto-grants-2010_05 |
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