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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2378648Generated: November 1, 2026

Bromine → 2-(S)-(2-Acetoxymethyl-4-amino-5-bromo-3-methyl-benzyl)-succinic acid diethyl ester

https://huagongshe.com/reaction/2378648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium AcetateHCID 517045—
Reactant2-(S)-(2-Acetoxymethyl-4-amino-3-methyl-benzyl)-succinic acid diethyl esterHCID 59731927—
SolventAcetic AcidHCID 176—
Product2-(S)-(2-Acetoxymethyl-4-amino-5-bromo-3-methyl-benzyl)-succinic acid diethyl esterHCID 5973188077%

Reaction Steps

2-(S)-(2-Acetoxymethyl-4-amino-3-methyl-benzyl)-succinic acid diethyl ester (7.6 g, 21 mmol) was dissolved in acetic acid (100 mL). Sodium acetate (4.2 g, 51 mmol) was added to the solution. Reaction vessel was placed in a cool water bath to control reaction exotherm. Bromine (1.1 mL, 22 mmol) was added to the mixture in one portion. Reaction stirred at ambient temperature for 10 minutes. Mixture was poured into 1N aqueous sodium thiosulfate solution (400 mL). Material was extracted twice with ethyl acetate. Organic phase was washed successively with water and brine. Organic was dried (magnesium sulfate), filtered and concentrated in vacuo. Silica gel chromatography (ethyl acetate-hexanes) afforded the desired product in 77% yield as an amber oil. MS m/e (M−H)−=440.0, 442.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07470679B2
Source datasetuspto-grants-2008_12
ORD IDord-608d8cf768d641e0ab0589a829d46647
Source noteuspto-grants-2008_12