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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781460Generated: October 31, 2026

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

https://huagongshe.com/reaction/1781460

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 numberUS05633287
Source datasetuspto-grants-1997_05
ORD IDord-c09943d57a0e41e9be3779e433d8d863
Source noteuspto-grants-1997_05