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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177751Generated: October 29, 2026

Sodium Bicarbonate → Ethyl 6-(4-chlorobenzenesulphonylmethyl)-3-bromo-2-methoxybenzoate

https://huagongshe.com/reaction/2177751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium 4-chlorobenzenesulfinateHCID 23664783—
ReactantEthyl 3-bromo-6-(dibromomethyl)-2-methoxybenzoateHCID 67107936—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductEthyl 6-(4-chlorobenzenesulphonylmethyl)-3-bromo-2-methoxybenzoateHCID 6710751057.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of ethyl 3-bromo-6-(dibromomethyl)-2-methoxybenzoate (Intermediate 88, 0.25 g), sodium bicarbonate (0.122 g) and sodium 4-chlorobenzenesulphinate (0.29 g) in dimethylacetamide (4 ml) and water (1 ml) was stirred and heated at 90° C. for 5 hours. After cooling, the mixture was diluted with water and loaded onto a water washed C-18 column which was then flushed with water and eluted with DCM and ethyl acetate. The organic eluent was dried (MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was purified by chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane with a gradient of 0-100% to give ethyl 6-(4-chlorobenzenesulphonylmethyl)-3-bromo-2-methoxy-benzoate (0.15 g) as a gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067905B2
Source datasetuspto-grants-2015_06
ORD IDord-61bd7d8e4d4847a8bb78613cbf6fdf5c
Source noteuspto-grants-2015_06