HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68612Generated: October 29, 2026
Triethylamine → HCID 66868579, compound
https://huagongshe.com/reaction/68612
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluorobenzenesulfonyl chloride | HCID 9588 | — |
| Reactant | t-Butyl 2-(2-(4-fluoro-3-(methylsulfonyl)phenyl)-4-((methylamino)methyl)phenoxy)acetate | HCID 67528897 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66868579 | HCID 66868579 | 73.7% |
Reaction Steps
To secondary amine 30 (150 mg, 0.35 mmol, 1 eq.) in dry DCM (15 mL) at 0° C. was added Et3N (3 mL) followed by dropwise addition of a DCM solution of 4-fluorobenzenesulfonyl chloride (90 mg, 0.42 mmol, 1.2 eq). After stirring at 0° C. for 20 min, the mixture was stirred at room temperature for 2 h. The reaction was extracted between DCM and water and the organic layer was washed with 1N HCl, saturated NaHCO3 solution, and brine, dried (Na2SO4), and concentrated in vacuo to give 150 mg (72%) of t-butyl 2-((4-fluoro-3-(methylsulfonyl)phenyl)-4-((4-fluoro-N-methylphenylsulfonamido)methyl)phenoxy)acetate (31) as oil which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822467B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-6217006d55254ab6952b54688f3fabdd |
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| Source note | uspto-grants-2014_09 |
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