HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 89851731, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 61392703 | HCID 61392703 | — |
| Product | HCID 89851731 | HCID 89851731 | — |
Reaction Steps
To a solution of 4,4,4-trifluoro-1-(2-methoxyphenyl)butan-2-one (6 g, 25.8 mmol, synthesized as in example 52, step 1) in MeOH (100 ml) was added NaBH4 (1.47 g, 38.7 mmol) at 0° C. and stirred for 1 h at RT. Then the reaction mixture was quenched with MeOH and concentrated under reduced pressure to afford crude compound. The title compound was purified by separation methods A, E and H. Yield (1.7 g). The enantiomer showed up at tr=12.8 min with Chiralpak 1A (4.6×250 mm) 5μ, hexane:2-PrOH:TFA (90:10:0.1), 1 ml/min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249127B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-444cfc1d9a7d409c9b2a22ee8afab88a |
| Source note | uspto-grants-2016_02 |