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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217440Generated: October 29, 2026

Water → Methyl 4-(Bromomethyl)-2-[(tert-butyldimethylsilyl)oxy]benzoate

https://huagongshe.com/reaction/217440

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-((tert-butyldimethylsilyl)oxy)-4-methylbenzoateHCID 58438769—
SolventCarbon TetrachlorideHCID 5943—
ProductMethyl 4-(Bromomethyl)-2-[(tert-butyldimethylsilyl)oxy]benzoateHCID 5843892787%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of methyl 2-{[tert-butyl(dimethyl)silyl]oxy}-4-methylbenzoate (3.4 g) in carbon tetrachloride (68 mL) were added, and NBS (2.16 g) and AIBN (398 mg) were added thereto at room temperature, followed by stirring at 80° C. for 1 hour. Completion of the reaction was confirmed by means of TLC, and to the reaction liquid was added water to stop the reaction, followed by extraction with EtOAc. The organic layer was washed with brine, dried using MgSO4, and then concentrated under reduced pressure, followed by purification by silica gel column chromatography (automatic purification device, hexane:EtOAc=100:0 to 95:5) to obtain methyl 4-(bromomethyl)-2-{[tert-butyl(dimethyl)silyl]oxy}benzoate (3.79 g) as a colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193378B2
Source datasetuspto-grants-2012_06
ORD IDord-0f7d09ec63144a56b65de87ea9d3cf80
Source noteuspto-grants-2012_06