HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Pentyl-3-cyclohexen-1-methanol toluenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 4-Pentyl-3-cyclohexen-1-methanol | HCID 19734035 | — |
| Product | 4-Pentyl-3-cyclohexen-1-methanol toluenesulfonate | HCID 19734042 | — |
Reaction Steps
To a solution of 4-pentyl-3-cyclohexen-1-methanol (3.0 g) in pyridine (3.3 ml) at 0° C. was added p-toluenesulfonyl chloride (3.3 g). The reaction was stirred in an ice bath for 2 hours, and then stored at -20 ° C. for a further 16 hours. The reaction mixture was then poured into 2 M HCl (75 ml) and extracted with ethyl acetate. The combined organic layers were extracted with saturated sodium chloride and dried over sodium sulfate. The solvent was removed in vacuo to produce 4-pentyl-3-cyclohexen-1-methanol toluenesulfonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05271864 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-ae801b14e8a045ceb9b70ec58a74af77 |
| Source note | uspto-grants-1993_12 |