HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672409Generated: October 30, 2026
Acetyl chloride → Acetamide, N-(2-methoxyphenyl)-
https://huagongshe.com/reaction/1672409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 2-Methoxyaniline | HCID 7000 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Product | Acetamide, N-(2-methoxyphenyl)- | HCID 7135 | — |
Reaction Steps
Ortho anisidine (0.67 moles, 82 g.) was taken in a 1 L round bottom flask equipped with a liquid addition funnel and a guard tube; triethylamine (1.0 mole, 100 g) was added to it in one lot. Above mixture was cooled to 0-5° C. and acetyl chloride was added drop-wise maintaining temperature below 10° C. After addition of acetyl chloride cooling was removed and the reaction mixture was stirred at 25-28° C. for 0.3 hours. After the completion of reaction (TLC), the reaction mixture was poured on ice-water, and aqueous layer was extracted with dichloromethane (2×300 mL). The combined dichloromethane extracts were then washed with water, brine and dried over anhydrous magnesium sulfate. The volatiles were removed under the reduced pressure to obtain 96.5 g. of solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998981B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-8bb8c555e1da4862b4a9456a0aafc4c9 |
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| Source note | uspto-grants-2011_08 |
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