HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889539Generated: October 29, 2026
Pivaloyl chloride → Methyl 2-chloro-5-(pivalamidomethyl)benzoate
https://huagongshe.com/reaction/889539
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 5-(aminomethyl)-2-chlorobenzoate--hydrogen chloride (1/1) | HCID 66524840 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2-chloro-5-(pivalamidomethyl)benzoate | HCID 67971274 | — |
Reaction Steps
To a thermally controlled reactor, add methyl 5-(aminomethyl)-2-chlorobenzoate hydrochloride (700 g, 3.51 mol, 1.0 equiv), dichloromethane (4.9 L), and N,N-diisopropylethylamine (1.71 L, 9.82 mol, 2.8 equiv). Add pivaloyl chloride (515 mL, 4.21 mol, 1.2 equiv) dropwise at such a rate that the internal temperature does not exceed 21° C. Upon completion of the addition, stir the reaction mixture at room temperature for one hour. Quench the reaction mixture with saturated aqueous sodium bicarbonate (10 L). Extract the mixture with dichloromethane (2×1 L), combine the organic extracts, dry over sodium sulfate, filter, and concentrate under reduced pressure to give an oil, (1.1 kg) carried on crude without further purification. MS (m/z) (35Cl/37Cl) 284/286 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252831B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-ed7f2283204a4d09957d66ddb8023f65 |
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| Source note | uspto-grants-2012_08 |
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