HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(M-Tolyl)propyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-(3-Methylphenyl)propan-1-ol | HCID 10261251 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(M-Tolyl)propyl methanesulfonate | HCID 53965794 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
3-(m-Methylphenyl)-1-propanol (0.45 g, 3.00 mmol), MsCl(278 uL, 3.60 mmol) and Et3N (0.84 mL, 6.00 mmol) were combined in CH2Cl2 (30 mL) and stirred at 0° C. for 4 hrs. The reaction was then diluted with CH2Cl2 (30 mL) and washed with cold brine, dried over Na2SO4 and concentrated to give a light brown oil. This was used without further purification. 1H NMR (300 MHz, CDCl3) δ 2.04-2.09 (m, 2H), 2.33(s, 3H), 2.69-2.74 (t, 2H), 2.99 (s, 3H), 4.20-4.24 (t, 2H), 6.97-7.04 (m, 3H), 7.16-7.19 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559172B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-a60fb841029445dcb957ebd85e14e7f2 |
| Source note | uspto-grants-2003_05 |