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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383158Generated: October 31, 2026

Carbon tetrabromide → N-[Bromomethyl-2-(2-methylphenyl)benzoyl]methionine methyl ester

https://huagongshe.com/reaction/383158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
ReactantN-[4-Hydroxymethyl-2-(2-methylphenyl)benzoyl]methionine methyl esterHCID 54396972—
SolventDichloromethaneHCID 6344—
ProductN-[Bromomethyl-2-(2-methylphenyl)benzoyl]methionine methyl esterHCID 54218056—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a stirred solution at −10° C. under N2 of N-[4-hydroxymethyl-2-(2-methylphenyl)benzoyl]methionine methyl ester (200 mg, 0.517 mmol ), prepared as in Example 403F, and carbon tetrabromide (189 mg, 0.568 mmol) in CH2Cl2 (5 mL) was added triphenylphosphine (163 mg, 0.620 mmol). Reaction stirred one hour at −10° C., and then, solvents concentrated in vacuo to produce a colorless glass. The residue could not be stored, and so, was used directly in the reaction in Example 1188B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310095B1
Source datasetuspto-grants-2001_10
ORD IDord-73b1fa7a316d40e3a8a5a23554bc9d61
Source noteuspto-grants-2001_10