HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863839Generated: October 29, 2026
Triethylamine → 6-Phenylhex-1-yl methylsulfonate
https://huagongshe.com/reaction/863839
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 6-Phenyl-1-hexanol | HCID 520110 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Phenylhex-1-yl methylsulfonate | HCID 13079702 | — |
Reaction Steps
To 6-phenyl-1-hexanol (3.2 g; 18 mmol) dissolved in CH2Cl2 (60 ml) is added Et3N (3.7 ml) and the solution is cooled to 0° C. Methanesulfonyl chloride (1.5 ml; 20 mmol) is added dropwise and then the reaction mixture is allowed to stir for 30 minutes at 0° C. This is then diluted with Et2O and washed with 2N HCl, NaHCO3 solution 2× and brine, dried (MgSO4) and concentrated to dryness to obtain 6-phenylhex-1-yl methylsulfonate as an oil which is used directly in Step E
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05561143 |
|---|
| Source dataset | uspto-grants-1996_10 |
|---|
| ORD ID | ord-f3ef825100d1416087fda81946c3c6aa |
|---|
| Source note | uspto-grants-1996_10 |
|---|