HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196456Generated: October 30, 2026
3'-Bromoacetophenone → 2-(3-Bromophenyl)propan-2-ol
https://huagongshe.com/reaction/2196456
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3'-Bromoacetophenone | HCID 16502 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Butyl ether | HCID 8909 | — |
| Product | 2-(3-Bromophenyl)propan-2-ol | HCID 15072383 | — |
Reaction Steps
Under an argon stream, 6.5 g of 3-bromoacetophenone are placed in a round-bottomed flask and dissolved in 544 ml of diethyl ether and 272 ml of tetrahydrofuran. The mixture is cooled to 0° C. using an ice bath, and 100 ml of a 1M solution of methylmagnesium bromide in dibutyl ether are added thereto, dropwise. The mixture is stirred at 0° C. for 1 h and 400 ml of a saturated aqueous solution of ammonium chloride are added. The organic phase is separated, dried over magnesium sulphate and concentrated under reduced pressure. 10.0 g of compound are obtained. 1H NMR (DMSO-d6, δ in ppm): 1.45 (s, 6H); 5.15 (s, 1H); 7.25 (t, 1H); 7.4 (d, 1H); 7.45 (d, 1H); 7.65 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08338451B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-b045dd1ce6884783a0ad8783d49cafee |
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| Source note | uspto-grants-2012_12 |
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