HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121203Generated: November 2, 2026
Oxalyl chloride → (4-Bromomethyl-2-phenylbenzoyl)methionine methyl ester
https://huagongshe.com/reaction/2121203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | L-Methionine, methyl ester, hydrochloride | HCID 11435579 | — |
| Reactant | 4-Bromomethyl-2-phenylbenzoic acid | HCID 23436455 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Bromomethyl-2-phenylbenzoyl)methionine methyl ester | HCID 54323738 | 75% |
Reaction Steps
To a solution in dichloromethane (25 mL) of 4-bromomethyl-2-phenylbenzoic acid (2.16 g, 7.42 mmol), prepared as in Example 234B, was added oxalyl chloride (0.84 mL, 965 mmol) and 2 drops on DMF and the reaction mixture was stirred for 2 hours. The reaction mixture was concentrated in vacuo and azeotroped with toluene. The residue was dissolved in dichloromethane (15 mL) and then was added to a solution in dichloromethane (15 mL) of methionine methyl ester hydrochloride (1.78 g, 8.90 mmol) and diisopropylethylamine (3.10 g, 17.81 mmol) (prepared at −10° C.) dropwise. The reaction mixture was stirred for 30 minutes and then was poured into ether and extracted with water, aqueous 3N HCl (2×) and brine, dried, filtered and concentrated in vacuo. Chromatography on silica gel (5% ethyl acetate-chloroforn) to give (4-bromomethyl-2-phenylbenzoyl)methionine methyl ester (2.42 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06693123B2 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-6535fdc3bacd48aea04de25869f6359c |
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| Source note | uspto-grants-2004_02 |
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