HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1848733Generated: October 25, 2026
Boron tribromide → Ethyl 3-(1-(4-bromobenzyl)-6-hydroxy-1H-benzo[d]imidazol-2-yl)-2,2-dimethylpropanoate
https://huagongshe.com/reaction/1848733
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | ethyl 3-(1-(4-bromobenzyl)-6-methoxy-1H-benzo[d]imidazol-2-yl)-2,2-dimethylpropanoate | HCID 90410153 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-(1-(4-bromobenzyl)-6-hydroxy-1H-benzo[d]imidazol-2-yl)-2,2-dimethylpropanoate | HCID 90411063 | — |
Reaction Steps
To a solution of ethyl 3-(1-(4-bromobenzyl)-6-methoxy-1H-benzo[d]imidazol-2-yl)-2,2-dimethylpropanoate (12 g, 27 mmol) in DCM (200 mL) was added BBr3 (20 g, 81 mmol) in DCM (100 mL) drop wise at −78° Celsius. The solution was gradually warmed to 5° Celsius and stirred for 3 h. The reaction mixture was slowly added to saturated NaHCO3 with rapid stirring for 1 h. The organic phase was separated and aqueous phase was extracted with DCM (200 mL). The combined organic phases were dried over Na2SO4, filtered, concentrated to dryness and purified by FCC to provide the title compound. MS (ESI): mass calcd. for C21H23BrN2O3, 430.09; m/z found, 438 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952177B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b355d2a73272492fb1433438377e49d9 |
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| Source note | uspto-grants-2015_02 |
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