HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384218Generated: November 2, 2026
Water → 3-(4-Bromophenyl)-2-methylpropan-1-ol
https://huagongshe.com/reaction/1384218
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Diboron | HCID 6328200 | — |
| Reactant | 3-(4-Bromophenyl)-2-methylpropanoic acid | HCID 21714191 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Bromophenyl)-2-methylpropan-1-ol | HCID 21714199 | 102% |
Reaction Steps
Diborane (192 ml of a 1.0 M solution in THF) was added dropwise over 25 minutes to a solution of 2-methyl-3-(4-bromophenyl)propanoic acid (38.9 g) in THF (240 ml) at 0° C. The reaction mixture was stirred for 45 minutes at 0° C. and then allowed to warm to ambient temperature over 2 hours. Water (120 ml) was added followed by solid potassium carbonate (144 g) and then more water (80 ml). The reaction mixture was extracted with diethyl ether (3×250 ml), the combined organic layers were dried (MgSO4) and the solvent was evaporated to give 2-methyl-3-(4-bromophenyl)propanol as a yellow oil (37.4 g), mass spectrum (+ve CI): 248 (M+NH4)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06258817B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-af0d0cb88da74749bbb8d576a35f3c39 |
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| Source note | uspto-grants-2001_07 |
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