HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893354Generated: November 3, 2026
Chlorosuccinimide → HCID 178501059, compound
https://huagongshe.com/reaction/1893354
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 178501060 | HCID 178501060 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178501059 | HCID 178501059 | 89.2% |
Reaction Steps
A solution of trans-4-(4-methyl-oxazol-2-yl)-cyclohexanecarboxylic acid methyl ester (277 mg, 1.24 mmol) and N-chlorosuccinimide (182 mg, 1.36 mmol) in N,N-dimethylformamide (2.5 ml) was stirred for 6 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 one 25-ml portion of tert-butyl methyl ether. The combined organic layers were washed with three 25-ml portions of water, dried over anhydrous sodium sulfate and concentrated in vacuo to give the crude title compound (285 mg, 89%) as light yellow solid, which was used in the next step without further purification. MS m/e: 258 ([M+H]+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08513238B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-08fe932b58f34c7a83c9ef7b04a07b1b |
|---|
| Source note | uspto-grants-2013_08 |
|---|