HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418611Generated: October 31, 2026
Cyclohexylamine → HCID 17805634, compound
https://huagongshe.com/reaction/418611
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexylamine | HCID 7965 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl malonyl chloride | HCID 123460 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | HCID 17805634 | HCID 17805634 | 97% |
Reaction Steps
To a solution of methyl 3-chloro-3-oxopropanoate (2.2 g, 16.1 mmol) in dry DCM (30 ml) at 0° C. was added cyclohexylamine (4.0 g, 40.3 mmol). The reaction mixture was stirred for 1 hr at room temperature. The reaction mixture was washed with diluted HCl, saturated NaHCO3 then brine well. The organic phase was collected, dried over anhydrous sodium sulfate then filtered and concentrated. The resultant crude amide was used directly in the next step with no additional purification (3.2 g, 100%). To a solution of this material (500 mg, 2.51 mmol) in THF/water (1:1, 20 ml) was added NaOH (200 mg, 5.02 mmol) and the mixture was stirred for 3 hrs at room temperature. The mixture was extracted with Et2O then the aqueous phase was acidified to pH 1 and extracted with EtOAc. The organic phase was collected, dried over anhydrous sodium sulfate then filtered and concentrated to afford the title compound 58 as a beige solid (450 mg, 97% yield). MS (m/z): 186.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093264B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-643450c6670648cdabb4c159fafc72b0 |
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| Source note | uspto-grants-2012_01 |
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