HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → {(1R,6S)-6-[(Benzyloxy)methyl]cyclohex-3-en-1-yl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | cis-1,2-Dihydroxymethylcyclohex-4-ene | HCID 11275057 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {(1R,6S)-6-[(Benzyloxy)methyl]cyclohex-3-en-1-yl}methanol | HCID 67946542 | 62.3% |
Reaction Steps
The diol (1) (16.2 g) in dimethylformamide (50 ml) is added dropwise to sodium hydride (3.1 g) in dimethylformamide (DMF) (50 ml). The mixture is stirred for 20 minutes and then benzyl chloride (16 g) is added and stirring is continued for a further 18 hours at 70° C. After removing the DMF in vacuo, water is added and the mixture is extracted with ether. The combined extracts are dried (MgSO4) and the solvent is evaporated to give a residue which is distilled under reduced pressure to give the title compound as an oil (16.5 g, ca. 60%), b.p. 140°-145° C./0.03 mm, νmax (film) 3440 and 1600 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04945106 |
| Source dataset | uspto-grants-1990_07 |
| ORD ID | ord-e40d7340a55643fab3198515ca37b132 |
| Source note | uspto-grants-1990_07 |