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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661652Generated: November 1, 2026

Potassium Carbonate → 4-[4-Bromo-5-chloro-2-(methyl-o-tolyl-carbamoyl)-phenoxy]-butyric acid tert-butyl ester

https://huagongshe.com/reaction/661652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-Butyl 4-bromobutanoateHCID 2757253—
Reactant5-bromo-4-chloro-2-hydroxy-N-methyl-N-o-tolyl-benzamideHCID 68602612—
SolventDimethylformamideHCID 6228—
Product4-[4-Bromo-5-chloro-2-(methyl-o-tolyl-carbamoyl)-phenoxy]-butyric acid tert-butyl esterHCID 6860272282.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

To 5-bromo-4-chloro-2-hydroxy-N-methyl-N-o-tolyl-benzamide (2.6 g, 7.3 mmol) in dry DMF (30 mL), was added K2CO3 (2.0 g, 7.6 mmol), followed by addition of t-butyl 4-bromobutyrate (2.0 g, 8.8 mmol). The mixture was heated at 60° C. for 12 hrs and partitioned between ethyl acetate and water. The organic layer was separated, washed with water and brine, and dried over MgSO4. After filtration, concentration and purification by silica gel column chromatography eluting with ethyl acetate in hexanes (3/7) gave 4-[4-bromo-5-chloro-2-(methyl-o-tolyl-carbamoyl)-phenoxy]-butyric acid tert-butyl ester (3.0 g). MS: 496.3 (M+H); tR=2.81 min (method 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084614B2
Source datasetuspto-grants-2011_12
ORD IDord-9d0fa683945041bcb8246647df2f2e5c
Source noteuspto-grants-2011_12