HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696300Generated: October 26, 2026
Acetyl chloride → ethyl 4-acetyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate
https://huagongshe.com/reaction/1696300
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ethyl 3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate | HCID 31090 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 4-acetyl-3,4-dihydro-2H-1,4-benzoxazine-2-carboxylate | HCID 13425083 | 66.7% |
Reaction Steps
Acetyl chloride (23 L, 0.33 mmol) was added to a solution of (±)-ethyl 3,4-dihydro-2H-benzo[b][1,4]oxazine-2-carboxylate (Example 3a, 55 mg, 0.27 mmol), DMAP (1.6 mg, 0.013 mmol), and Hunig's base (63 L, 0.36 mmol) in dichloromethane (2 mL). The solution was stirred at 25° C. for 24 h, then the reaction mixture was diluted with dichloromethane (60 mL) and the mixture was extracted with 0.1 M sodium carbonate (7 mL) and half-saturated brine (7 mL). The organic layer was dried over sodium sulfate and concentrated. Purification of the product by flash column chromatography (40% EtOAc/hexane) afforded the title compound (46 mg, 0.18 mmol). MS m/z: 250 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163766B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-d9b93c1dee6f47228a481e2b53d3e33d |
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| Source note | uspto-grants-2012_04 |
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