HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324749Generated: October 28, 2026
p-Bromoacetophenone → (S)-4-Bromo-alpha-methylbenzyl alcohol
https://huagongshe.com/reaction/324749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | 1-(4-Bromophenyl)ethanol | HCID 95352 | — |
| Reactant | (R)-1-(4-Bromophenyl)ethanol | HCID 6950173 | — |
| Product | (S)-4-Bromo-alpha-methylbenzyl alcohol | HCID 2734890 | 57% |
Reaction Steps
As shown here, the biochemical conversion reaction of immobilized green pea protein for the substrate (±)-1-(4-bromophenyl)ethanol (200 mg) requires 8 days by going through bioconversion to 4-bromoacetophenone accompanying sterically selective oxidation of (R)-1-(4-bromophenyl)ethanol to obtain 114 mg of (S)-1-(4-bromophenyl)ethanol at a yield of 57%. Optical purity was obtained at 88% e.e. The reaction course and time at completion of reaction were determined by GC using the Hitachi Model G-3500 gas chromatograph under conditions consisting of carrier gas: He at 0.48 ml/min, split ratio: 1/55, oven temperature: 150° C., inlet temperature: 250° C., outlet temperature: 250° C., pressure: 136, flow rate value: 42, analytical column: TC-5HT 0.25 mm I.D.×30M df (GL Science).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06218581B1 |
|---|
| Source dataset | uspto-grants-2001_04 |
|---|
| ORD ID | ord-6d592d36f9614b30912d0e74865dc794 |
|---|
| Source note | uspto-grants-2001_04 |
|---|