HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(2-Bromophenyl)ethyl behenate → 1-(2-Bromophenyl)ethan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(2-Bromophenyl)ethyl behenate | HCID 21468172 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(2-Bromophenyl)ethan-1-ol | HCID 6950331 | 88% |
Reaction Steps
Interesterification was carried out by using 3 g of Lipase QL, 50 g of (R,S)-1-(2-bromophenyl)ethanol, and 150 g of tribehen at 120° C. for 20 hours in the same manner as in Example 12. The water content of the reaction system was 0.01% by weight, and 90% of the lipase particles had a particle size of 30 to 50 μm. Gas chromatography of the reaction mixture revealed that 44 mol % of (R,S)-1-(2-bromophenyl)ethanol had been converted to 1-(2-bromophenyl)ethyl behenate. The reaction mixture was treated in the same manner as in Example 12, and the filtrate was subjected to simple distillation at 110° C. and 5 mmHg to recover unreacted (S)-(-)-1-(2-bromophenyl)ethanol (yield: 88%; chemical purity: 99.9%; optical purity: 99% ee or higher).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05696299 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-cc88f2f51df940b8936dbb7e7a8ad1f1 |
| Source note | uspto-grants-1997_12 |