HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527722Generated: 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/1527722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| 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 | 60% |
Reaction Steps
A solution of boron tribromide (3.1 mL, 1 M in DCM) was added drop-wise to a 100 mL round bottomed flask containing ethyl 3-(1-(4-bromobenzyl)-6-methoxy-1H-benzo[d]imidazol-2-yl)-2,2-dimethylpropanoate (700 mg, 1.6 mmol) and DCM (30 mL) at −78° Celsius. The resulting solution was allowed to warm to 5° Celsius over 3 h and partitioned with sat. NaHCO3 (50 mL). The aqueous layer was extracted with DCM (3×25 mL). The combine organic layers were dried with sodium sulfate, filtered, and concentrated to dryness. The residue was subjected to FCC to give the title compound (410 mg, 60%). MS (ESI): mass calcd. for C21H23BrN2O3, 430.08; m/z found, 431.0 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09089569B2 |
|---|
| Source dataset | uspto-grants-2015_07 |
|---|
| ORD ID | ord-d3ffddc99a8641baa33e50464ec8a48a |
|---|
| Source note | uspto-grants-2015_07 |
|---|