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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396263Generated: October 30, 2026

Triethylamine → N-(2,4,6-triisopropylbenzylsulfonyl)-2-(2,6-diisopropylphenyl)acetamide

https://huagongshe.com/reaction/2396263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4,6-TriisopropylbenzylsulfonamideHCID 19046539—
Reactant2,6-Diisopropylphenylacetyl chlorideHCID 19362782—
SolventTetrahydrofuranHCID 8028—
ProductN-(2,4,6-triisopropylbenzylsulfonyl)-2-(2,6-diisopropylphenyl)acetamideHCID 982809812.1%

Reaction Steps

A solution of 2,4,6-triisopropylbenzylsulfonamide (100 mg, 0.33 mmol), 2,6-diisopropylphenylacetyl chloride (75 mg, 0.34 mmol), and Et3N (47 μL, 0.34 mmol) in 10 mL THF was stirred at room temperature overnight. The solvent was evaporated and the residue was distributed between ethyl acetate and 0.1N HCl, the organic layer was washed with brine, dried, and evaporated. The pure product (20 mg, 12%) was isolated by column chromatography (4:1 hexane:EtOAc), m/e=499; NMR (CDCl3): δ 7.05-7.4 (m, 5H), 4.25 (s, 2H), 3.95 (s, 2H), 3.45-3.6 (m, 1H), 3.0-3.15 (m, 2H), 2.85-3.0 (m, 2H), 1.05-1.4 (m, 30H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05491172
Source datasetuspto-grants-1996_02
ORD IDord-939e5efd586a4a8e9223a309e9555aaf
Source noteuspto-grants-1996_02