HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096822Generated: October 25, 2026
Methanol → Benzenemethanol, 3,5-dichloro-4-hydroxy-
https://huagongshe.com/reaction/1096822
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 3,5-Dichloro-4-hydroxybenzoic acid | HCID 18749 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzenemethanol, 3,5-dichloro-4-hydroxy- | HCID 176409 | — |
Reaction Steps
BH3 (1M in THF, 250 mL, 250 mmol) was added dropwise to a cooled sol. of 3,5-dichloro-4-hydroxybenzoic acid (20 g, 96.6 mmol) in THF (200 mL) at 0° C. The resulting mixture was stirred at 0° C. for 15 min., and then at rt for 13 h. The milky mixture was cooled to 0° C., and MeOH (150 mL), then water (100 mL), were added dropwise. The mixture was further stirred at 0° C. for 15 min, and then at rt for 5 h. The mixture was then partially concentrated under reduced pressure. EtOAc (200 mL) and water (50 mL) were added to the residue, and the phases were shaken and separated. The aq. phase was further extracted with EtOAc. The combined org. extracts were washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure. Purification by FC(CH2Cl2/CH3OH, 100:1) led to the title compound as a slightly beige solid (17.86 g, 96%). LC-MS: tR=0.69 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138340B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-90e996b781944c7a9eb2dd649fbe0bcb |
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| Source note | uspto-grants-2012_03 |
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