HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Methoxypropyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-Methoxy-1-propanol | HCID 74116 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Methoxypropyl methanesulfonate | HCID 11693963 | 97% |
Reaction Steps
Methanesulphonyl chloride (1.75 ml, 22 mmol) was added to a solution of 3-methoxy-1-propanol (1.81 g, 20 mmol) and triethylamine (3.35 ml, 24 mmol) in DCM (40 ml) cooled in an ice bath and the mixture stirred at ambient temperature for 18 hours. DCM (25 ml) and water (50 ml) were added and the phases separated and the aqueous layer was extracted with DCM (25 ml). The extracts were combined, washed with water (50 ml) and brine (50 ml), dried (Chemelut column CE1010) and evaporated to give the title compound 3.25 g (97%) as a pale yellow oil. NMR 2.00 (m, 2H), 3.01 (s, 3H), 3.35 (s, 3H), 3.49 (t, 2H), 4.38 (t, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969714B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-32664888bc4844b79042b075aefd7170 |
| Source note | uspto-grants-2005_11 |