HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788640Generated: November 1, 2026
Methanesulfonyl chloride → HCID 20189890, compound
https://huagongshe.com/reaction/1788640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Propylbutane-1,4-diol | HCID 12508255 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 20189890 | HCID 20189890 | — |
Reaction Steps
Methanesulphonyl chloride (16.95 g) was added dropwise to a stirred solution of 3-hydroxymethylhexan-1-ol (8.94 g) in pyridine (39.5 g), maintaining the temperature at less than 5° C. Following the addition, the reaction mixture was stirred at 0° C. for 1.5 hours, then diluted with water and extracted with dichloromethane. The extracts were washed successively with water, dilute hydrochloric acid (X 2), water, aqueous sodium bicarbonate, and water, then dried over magnesium sulphate and concentrated to give 3-methanesulphonyloxymethylhex-1-yl methanesulphonate. (16.13 g, 83%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04684396 |
|---|
| Source dataset | uspto-grants-1987_08 |
|---|
| ORD ID | ord-b735e5a5475e4b5385211bc2dd514f1b |
|---|
| Source note | uspto-grants-1987_08 |
|---|