HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 178520638, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178520637 | HCID 178520637 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | HCID 178520638 | HCID 178520638 | 81.3% |
Reaction Steps
A solution of 0.44 g of 3-[trans-4-[(4'-fluoro-4-biphenylyl)ethynyl]cyclohexyl]propanal in 20 ml of methanol/water (vol. 4:1) and 15 ml of dioxan is treated portionwise with 0.10 g of sodium borohydride. The reaction mixture is stirred at room temperature for 0.75 hour and concentrated. The residue is treated with water and extracted with diethyl ether. The ether phase is washed with water, dried over sodium sulphate, filtered and evaporated. 0.36 g of 3-[trans-4-[(4'-fluoro-4-biphenylyl)ethynyl]cyclohexyl]propanol is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05447657 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-3b6163c6f28c4464847990d196772bbb |
| Source note | uspto-grants-1995_09 |