HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → α-Cyclopropyl-4-(methylthio)benzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Cyclopropyl[4-(methylsulfanyl)phenyl]methanone | HCID 13533274 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | α-Cyclopropyl-4-(methylthio)benzenemethanol | HCID 14988329 | 74.2% |
Reaction Steps
To 200 ml of methanol solution containing 24 g of cyclopropyl (4-methylthiophenyl)ketone was added slowly 9.4 g of sodium borohydride under an ice-cooled condition, the reaction mixture was stirred for 2 hours. Then an adequate amount of acetone was added to the reaction mixture and concentrated under a reduced pressure. To the residue thus obtained was added chloroform, and the chloroform solution was washed with water, dried with anhydrous sodium sulfate, and the solvent was removed by evaporation to yield 18 g of 1-(cyclopropyl, hydroxylmethyl)-4-methylthiobenzene as in the form of colorless oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05137889 |
| Source dataset | uspto-grants-1992_08 |
| ORD ID | ord-5103d4df205549d684f7607cc47b20fd |
| Source note | uspto-grants-1992_08 |