HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218331Generated: October 29, 2026
Boron trifluoride etherate → HCID 20631745, compound
https://huagongshe.com/reaction/2218331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-Bromo-2-(3,5-dimethoxyphenoxy)benzoic acid | HCID 23431860 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20631745 | HCID 20631745 | 64.5% |
Reaction Steps
To a solution of 75.4 g (F.W. 353.168, 213 mmol) of 4-bromo-2-(3,5-dimethoxyphenoxy)benzoic acid (22) in 300 mL of tetrahydrofuran was added 8.9 g (F.W. 37.83, 235 mmol) of sodium borohydride portionwise at room temperature and then, 31 mL (F.W. 141.93, d=1.154, 252 mmol) of boron trifluoride diethyl etherate was added thereto dropwise. The resulting solution was stirred at room temperature for one hour. To this reaction solution was added 200 mL of ice water slowly. The resulting solution was extracted with ethyl acetate and the extract was washed with a saturated sodium chloride aqueous solution three times. After drying with anhydrous magnesium sulfate, the solvent was removed under reduced pressure. The residue was recrystallized from benzene-diisopropyl ether to obtain 46.6 g (64%) of alcohol (23). (TLC; ethyl acetate:hexane=1:4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07410997B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-42104081c81043ecb554dfbc40b7ba2b |
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| Source note | uspto-grants-2008_08 |
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