HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896719Generated: October 30, 2026
2-Bromo-6-chlorobenzoic acid → Methyl 2-bromo-6-chlorobenzoate
https://huagongshe.com/reaction/896719
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-6-chlorobenzoic acid | HCID 33125 | — |
| Reactant | Trimethylsilyldiazomethane | HCID 167693 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-bromo-6-chlorobenzoate | HCID 2759827 | — |
Reaction Steps
To a solution of 2-bromo-6-chlorobenzoic acid (17.7 g, 75.2 mmol) in methanol (200 mL) at 0° C. was added (trimethylsilyl)diazomethane (2M in hexanes, 100 mL, 0.200 mol). The solution was stirred at 0° C. for 1.5 hours, then warmed to room temperature and washed with aqueous sodium bicarbonate and brine, dried over Na2SO4, filtered and concentrated. The residue was subjected to silica gel chromatography eluted with 0-5% ethyl acetate in hexanes to provide methyl 2-bromo-6-chlorobenzoate as a pale yellow oil that gave proton NMR spectra consistent with theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919343B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-461a62a34e8f4c24b67ae45093547b47 |
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| Source note | uspto-grants-2005_07 |
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