HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220394Generated: October 26, 2026
Isopropylethanediol → 2-Isopropoxyethyl Methanesulfonate
https://huagongshe.com/reaction/220394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropylethanediol | HCID 7996 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Isopropoxyethyl Methanesulfonate | HCID 18465045 | 126.4% |
Reaction Steps
A round bottom flask was charged with 2-isopropoxyethanol (0.5 mL, 4.34 mmol) and dichloromethane (21.68 mL) and was cooled to 0° C. Triethylamine (1.208 mL, 8.67 mmol) was added along with a tip of DMAP. Methanesulfonyl chloride (0.338 mL, 4.34 mmol) was added dropwise. The reaction mixture was slowly warmed to rt over 2 h. The reaction mixture was quenched with saturated aqueous ammonium chloride and transferred to a separatory funnel. The aqueous layer was extracted with dichloromethane (2×). The combined organics were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. 2-Isopropoxyethyl methanesulfonate (1 g) was isolated as a clear oil and was immediately used in the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202881B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-5dd2a2d8c64b4e20b81cc5e9e4f85b5f |
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| Source note | uspto-grants-2012_06 |
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