HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(4-Cyanophenyl)butyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(4-Hydroxybutyl)benzonitrile | HCID 18540380 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Cyanophenyl)butyl methanesulfonate | HCID 18540424 | — |
Reaction Steps
Methanesulfonyl chloride (2.32 mL, 30 mmol) was added to a cooled is (0° C.), stirred solution of 4-(4-hydroxybutyl)benzonitrile (from step (ii) above, 5.2 g, 29.7 mmol) and triethylamine (4.35 mL) in dichloromethane (50 mL). The resulting mixture was stirred for 4 h before water (150 mL) was added, and the organic layer separated, dried and concentrated to give the sub-title compound. This product was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07164017B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-edfef166958143b0bcc91c2e89d8d9cb |
| Source note | uspto-grants-2007_01 |