HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Hydroxymethyl-2-n-propyl propan-1,3-diol trimethanesulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Butylidynetrimethanol | HCID 81928 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Hydroxymethyl-2-n-propyl propan-1,3-diol trimethanesulphonate | HCID 86744882 | — |
Reaction Steps
Methanesulphonyl chloride (74.0 g) was added dropwise over 30 minutes to a solution of 2-hydroxymethyl-2-n-propylpropan-1,3-diol (28.0 g) in dry pyridine (200 ml) under nitrogen at 0° C. The mixture was allowed to warm to room temperature. After stirring for 18 hours the mixture was poured into water (200 ml) and extracted with chloroform (2×200 ml). The chloroform extracts were washed with water (2×100 ml), dried over anhydrous magnesium sulphate and evaporated in vacuo to give a brown solid. This was stirred in dry diethyl ether (200 ml) to give 2-hydroxymethyl-2-n-propylpropan-1,3-diol trimethanesulphonate as a white solid. (70.0 g)(m.pt.103.6°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466710 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-e63dbdcee095420d97b4d4030ddcaad7 |
| Source note | uspto-grants-1995_11 |