HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424362Generated: October 27, 2026
Methanol → (2-Bromo-5-chlorophenyl)methanol
https://huagongshe.com/reaction/424362
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Bromo-5-chlorobenzoic acid | HCID 89027 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Bromo-5-chlorophenyl)methanol | HCID 23363134 | 88.8% |
Reaction Steps
To a solution of 2-bromo-5-chlorobenzoic acid (5.49 g, 23.3 mmol) in anhydrous THF (70 mL) under nitrogen was added dropwise a BH3 THF solution (1.0 M, 55 mL) at 0° C. and the reaction mixture was stirred overnight at room temperature. Then the mixture was cooled on an ice bath and MeOH (20 mL) was added dropwise to decompose excess BH3. The resulting mixture was stirred until no bubble was released and then 10% NaOH (10 mL) was added. The mixture was concentrated and the residue was mixed with water (200 mL) and extracted with EtOAc. The residue from rotary evaporation was purified by silica gel column chromatography (5:1 hexane/EtOAc) to give 2-bromo-5-chlorobenzyl alcohol as a white solid (4.58 g, 88%): 1H NMR (300 MHz, DMSO-d6): δ (ppm) 7.57 (d, J=8.7 Hz, 1H), 7.50-7.49 (m, 1H), 7.28-7.24 (m, 1H), 5.59 (t, J=6.0 Hz, 1H), 4.46 (d, J=6.0 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106031B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-29759bc600d64eb9a34f7576918d991c |
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| Source note | uspto-grants-2012_01 |
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