HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893356Generated: October 31, 2026
N-bromobutanimide → HCID 178472352, compound
https://huagongshe.com/reaction/1893356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | HCID 178472356 | HCID 178472356 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178472352 | HCID 178472352 | 89% |
Reaction Steps
A solution of cis/trans-4-(4-methyl-thiazol-2-yl)-cyclohexanecarboxylic acid ethyl ester (1:5) (319 mg, 1.26 mmol) and N-bromosuccinimide (247 mg, 1.38 mmol) in N,N-dimethylformamide (1.6 ml) was stirred for 1 h at room temperature. The reaction mixture was partitioned between tert-butyl methyl ether (25 ml) and 0.1 M aqueous sodium hydroxide solution (25 ml). The layers were separated. The aqueous layer was extracted with two 25-ml portions of tert-butyl methyl ether. The combined organic layers were washed with two 25-ml portions of water, dried over anhydrous sodium sulfate and concentrated in vacuo to give the crude title compound (371 mg, 89%) as light yellow solid, which was used in the next step without further purification. MS m/e: 334 ([M+H]+)
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-8d71fd789fe0463296ea83f83c3f71d1 |
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| Source note | uspto-grants-2013_08 |
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