HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 2-(4-Phenoxyphenoxy)cyclopentan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(4-Phenoxyphenoxy)-cyclopentan-1-one | HCID 20385741 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Phenoxyphenoxy)cyclopentan-1-ol | HCID 22247676 | — |
Reaction Steps
A solution of 3.78 g of sodium borohydride in 10 ml of water is added at room temperature to a solution of 8.04 g of 2-(4-phenoxyphenoxy)-cyclopentan-1-one in 60 ml of methanol. The reaction mixture is stirred for 15 hours at room temperature and then concentrated under reduced pressure. The residue is poured into ice-water and extracted with ether. The organic phase is washed twice with saturated sodium chloride solution, dried over sodium sulphate and concentrated by rotary evaporation. Fractional distillation of the residue yields 2-(4-phenoxyphenoxy)-cyclopentan-1-ol as a colourless oil with a boiling point of 181°-185° C./0.001 torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04175137 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-2ef5f5af53484609ab6d59ece6adafd5 |
| Source note | uspto-grants-1979_11 |