HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514770Generated: October 30, 2026
Triethylamine → 2-{[(2-Nitrophenyl)sulfonyl]amino}ethyl methanesulfonate
https://huagongshe.com/reaction/514770
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | N-(2-hydroxyethyl)-2-nitrobenzenesulfonamide | HCID 3102011 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-{[(2-Nitrophenyl)sulfonyl]amino}ethyl methanesulfonate | HCID 86635903 | — |
Reaction Steps
Triethylamine (20 mL, 144.6 mmol) was added to a solution of compound 54 (29.5 g, 119.9 mmol) in ethyl acetate (300 mL). The mixture was cooled to 10° C. in an ice bath. Then, a solution of mesyl chloride (10.2 mL, 131.8 mmol) in ethyl acetate (50 mL) was added dropwise at a temperature ≦20° C. The resulting solution was stirred at room temperature for 3 h (TLC monitoring, eluent: hexane-ethyl acetate, 4:1). The reaction mixture was filtered to remove the precipitate-triethylamine hydrochloride. The filtrate was washed with aqueous NaHCO3, water, and evaporated. Yield of 55: 32.2 g (83%) as crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108916B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-612a917d996b4eb1b1be5063b1d96cbf |
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| Source note | uspto-grants-2015_08 |
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