HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272561Generated: October 25, 2026
Acetyl chloride → Methyl 3-Amino-4-chlorobenzoate
https://huagongshe.com/reaction/272561
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 3-Amino-4-chlorobenzoic acid | HCID 76092 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 3-Amino-4-chlorobenzoate | HCID 593055 | — |
Reaction Steps
To a solution of 4-chloro-3-amino-benzoic acid (10.0 g, 58.3 mmol) in methanol (50 mL) was added acetyl chloride (13.0 mL) dropwise at room temperature. After the addition, the reaction mixture was heated at 70° C. for 3 h and then cooled to room temperature. The solvent was removed under reduced pressure and water (100 mL) was added. The resulting solution was neutralized with NaHCO3 followed by extraction with EtOAc (3×100 mL). The combined organic layers were dried (MgSO4) and concentrated in vacuum to afford a yellow oil (22, 10.5 g, 97%). 1H NMR (DMSO-d6, 300 MHz) δ 7.41 (??d, J=2.1 Hz, 1H), 7.31 (d, J=8.4 Hz, 1H), 7.09 (dd, J=2.1, 8.4 Hz, 1H), 5.66 (br s, 2H), 3.80 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07456178B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-0cee1c864a20495cba821184f621b338 |
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| Source note | uspto-grants-2008_11 |
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