HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662336Generated: October 29, 2026
4-Bromo-3-(butyloxy)benzoic acid → (4-Bromo-3-(butyloxy)phenyl)methanol
https://huagongshe.com/reaction/1662336
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromo-3-(butyloxy)benzoic acid | HCID 57706230 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Bromo-3-(butyloxy)phenyl)methanol | HCID 57705850 | 102.2% |
Reaction Steps
A solution of 20.1 (0.68 g, 2490 μmol) in THF (5 mL) was treated with borane THF complex (4979 μL, 4979 μmol) and stirred overnight at 65° C. The reaction mixture was quenched with MeOH, diluted with EtOAc, and washed with water and brine. The organic layer was dried over Na2SO4 and concentrated. The crude product was purified by combiflash (10 to 50% EtOAc/hexanes) yielding 20.2 (659.3 mg, 102% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030354B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-742b83af6866476c8c5c823506a9982a |
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| Source note | uspto-grants-2011_10 |
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