HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893347Generated: October 30, 2026
Chlorosuccinimide → HCID 178501072, compound
https://huagongshe.com/reaction/1893347
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 178501043 | HCID 178501043 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178501072 | HCID 178501072 | 95.3% |
Reaction Steps
A solution of trans-4-(5-methyl-isoxazol-3-yl)-cyclohexanecarboxylic acid methyl ester (250 mg, 1.12 mmol) and N-chlorosuccinimide (164 mg, 1.23 mmol) in N,N-dimethylformamide (2.2 ml) was stirred for 24 h at room temperature. The reaction mixture was partitioned between tert-butyl methyl ether (50 ml) and water (50 ml). The layers were separated. The aqueous layer was extracted with one 50 ml-portion of tert-butyl methyl ether. The combined organic layers were washed with one 50 ml-portion of 0.1 M aqueous sodium hydroxide solution, one 50 ml-portion of water and one 30 ml-portion of brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give the crude title compound (275 mg, 95%) as light yellow oil, which was used in the next step without further purification. MS m/e: 257 (M+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513238B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-773f7a7ed7e54c6dbefbeba401b7c5de |
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| Source note | uspto-grants-2013_08 |
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