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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-((tert-butyldimethylsilyl)oxy)-4-methylbenzoate | HCID 58438769 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 4-(Bromomethyl)-2-[(tert-butyldimethylsilyl)oxy]benzoate | HCID 58438927 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193378B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-0f7d09ec63144a56b65de87ea9d3cf80 |
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| Source note | uspto-grants-2012_06 |
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