HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1008869Generated: October 26, 2026
Sodium Hydroxide → 3-(3-Bromophenyl)propan-1-ol
https://huagongshe.com/reaction/1008869
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-(3-bromophenyl)propanoic Acid | HCID 2063862 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(3-Bromophenyl)propan-1-ol | HCID 18785928 | — |
Reaction Steps
A suspension of 1.84 g (8 mmol) of 3-(3-bromophenyl)propionic acid and 0.91 g (24 mmol) of sodium borohydride in 20 ml of THF, cooled to 0° C., is admixed in small portions with 3.2 ml (25 mmol) of trifluoroborane-diethyl ether complex. Stirring is continued in the cold for 1 hour, and then at ambient temperature for 16 hours. The reaction mixture is cooled to 0° C. and neutralized to a pH of 7˜8 by adding a 1N solution of aqueous sodium hydroxide. It is concentrated under reduced pressure and then the residue is taken up in water. It is extracted with dichloromethane and dried over sodium sulphate. Following filtration, the organic phase is concentrated under reduced pressure. This gives 1.62 g (7.53 mmol) of product in the form of an oil, which is used as it is in the following step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07973042B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-660663bf28624fefb388f227bccf1031 |
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| Source note | uspto-grants-2011_07 |
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