HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818920Generated: November 1, 2026
4-Chlorobenzoyl chloride → HCID 43623645, compound
https://huagongshe.com/reaction/1818920
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | 2-Amino-5-methylbenzoic acid | HCID 76255 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 43623645 | HCID 43623645 | — |
Reaction Steps
To a solution of 2-amino-5-methyl benzoic acid (1.0 mmol) dissolved in 10% MeOH in toluene (2.5 mL) is added dropwise trimethylsilyl-diazomethane (2.0 M in hexanes, 0.75 mL). The reaction mixture is stirred at room temperature for 1 hour and the solvent is removed under reduced pressure. The resulting methyl ester is dissolved in dichloromethane (3.0 mL) and then 4-chlorobenzoyl chloride (1.0 equivalent) and DIEA (1.0 equivalent) is added sequentially. The reaction mixture is stirred for 3 hours and the solvent is evaporated. The yellow residue is diluted with EtOAc, washed with 1 M NaHSO4, brine, dried, filtered and concentrated under reduced pressure to provide 2-(4-chloro-benzoylamino)-5-methyl-benzoic acid methyl ester (compound 11.1) which is used without purification in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601725B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-e7a0b050c30c4a62a4e1478d99a5f8b0 |
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| Source note | uspto-grants-2009_10 |
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