HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466534Generated: October 26, 2026
Triethylamine → 2-Phenoxyethyl methanesulfonate
https://huagongshe.com/reaction/1466534
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenoxyethanol | HCID 31236 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenoxyethyl methanesulfonate | HCID 226499 | 99% |
Reaction Steps
To a solution of 2-phenoxyethanol (10.0 mL, 80.0 mmol) and triethylamine (13.5 mL, 96.9 mmol) in anhydrous CH2Cl2 (250 mL) at 0° C. is added methanesulfonyl chloride (6.80 mL, 87.9 mmol). The resulting cloudy mixture is stirred at 0° C. for 2 h. The mixture is diluted with water (75 mL) and extracted. The organic layer is washed with 1N HCl (75 mL) then saturated NaHCO3/brine (1:1; 75 mL) dried (Na2SO4), filtered, and concentrated. The residue is dried to constant weight under reduced pressure to provide the title compound as a pale yellow oil (17.1 g, 99%). This material is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09000043B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-cffced9ee9e14d54820506abb6707b2f |
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| Source note | uspto-grants-2015_04 |
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