HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483734Generated: October 30, 2026
Hydrochloric Acid → HCID 14517058, compound
https://huagongshe.com/reaction/483734
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 14517057 | HCID 14517057 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 14517058 | HCID 14517058 | — |
Reaction Steps
Sodium hydroxide solution (2 molar, 0.5 cm3) was added to a solution of 3-(2,4-difluorophenoxy)benzaldehyde (2 g) in methanol (20 cm3) and the mixture was cooled to 0° C. Sodium borohydride (0.5 g) was added, and the mixture stirred for 30 minutes. After this time, water was added, and the mixture acidified to pH 4 by addition of dilute hydrochloric acid. This mixture was extracted with diethyl ether (5×50 cm3). The combined organic layers were dried over anhydrous sodium sulphate, and the solvents evaporated under reduced pressure. The residue was purified by column chromatography on a silica gel support, using n-hexane containing 20% by volume ethyl acetate as eluent, to give 3-(2,4-difluorophenoxy)benzyl alcohol as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05225607 |
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| Source dataset | uspto-grants-1993_07 |
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| ORD ID | ord-349d5b704ae74a96834dc83f98523cd4 |
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| Source note | uspto-grants-1993_07 |
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