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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441Generated: October 26, 2026

N-t-butyl-3-(1-acetoxy-2-chloroethyl)-2-thiophenesulfonamide → 3-(1-Acetoxy-2-chloroethyl)-2-thiophenesulfonamide

https://huagongshe.com/reaction/1441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-t-butyl-3-(1-acetoxy-2-chloroethyl)-2-thiophenesulfonamideHCID 19690764—
SolventTrifluoroacetic acidHCID 6422—
Product3-(1-Acetoxy-2-chloroethyl)-2-thiophenesulfonamideHCID 1969077972%

Reaction Steps

1.5 g (0.0044 mole) of N-t-butyl-3-(1-acetoxy-2-chloroethyl)-2-thiophenesulfonamide synthesized in Example 7 was dissolved in 5 ml of trifluoroacetic acid. The reaction solution was stirred at normal temperature for 12 hours and then concentrated under reduced pressure. The residue was dissolved in methylene chloride and the solution was washed with aqueous sodium bicarbanate solution. The organic layer was separated, dried over anhydrous magnesium sulfate and filtered. The filtrate was then concentrated. The residue was subjected to column chromatograpy on silica gel to obtain 760 mg (Yield: 72%) of the pure title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05726127
Source datasetuspto-grants-1998_03
ORD IDord-8f3db3635526422b993dd23dd01d5b7e
Source noteuspto-grants-1998_03