HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418142Generated: October 31, 2026
Ethanesulfonyl chloride → HCID 19348792, compound
https://huagongshe.com/reaction/1418142
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanesulfonyl chloride | HCID 11667 | — |
| Reactant | HCID 19348478 | HCID 19348478 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19348792 | HCID 19348792 | 42.5% |
Reaction Steps
180 μl (1.90 mmol) of ethanesulfonyl chloride and then 213 mg (1.75 mmol) of 4-N,N-dimethylaminopyridine were added to a solution of 700 mg (1.59 mmol) of N-[2-t-butyl-5-(aminomethyl)phenyl]-3-(2,4-dimethoxyphenyl)octanamide (prepared as described in Preparation 26A) in 15 ml of methylene chloride, whilst cooling in an ice-salt bath, and the resulting mixture was stirred at the same temperature for 1 hour. At the end of this time, the reaction mixture was diluted with ethyl acetate, and the diluted solution was washed with water, with a saturated aqueous solution of sodium hydrogencarbonate and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and the resulting residue was purified by column chromatography through 38 g of silica gel, using a 3:1 by volume mixture of ethyl acetate and hexane as the eluent, to give 360 mg of the title compound as a foam-like substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05880147 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-d7fdb425c3de450a8cfa2ecdc1f01172 |
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| Source note | uspto-grants-1999_03 |
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