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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443227Generated: November 3, 2026

Ammonium Chloride → HCID 17989149, compound

https://huagongshe.com/reaction/1443227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
ReactantHCID 17989120HCID 17989120—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 17989149HCID 17989149—

Reaction Conditions

Temperature-70 °C

Reaction Steps

24.1 g (84.63 mmol) of ethyl-4-(4-chloro-3-methoxyphenyl)-4-methylpentanoate is dissolved in 296 ml of tetrahydrofuran, and the reaction mixture is cooled to −70° C. to −65° C. Within ¾ hour, 236.9 ml of a 0.5 molar solution of potassium-bis-(trimethylsilylamide) in toluene is added in drops, and the reaction mixture is then stirred for 75 more minutes at −70° C. 30.9 g (118.48 mmol) of Davis reagent, dissolved in 296 ml of tetrahydrofuran, is now added in drops within 60 minutes. After two hours of stirring at −70° C., 152 ml of saturated ammonium chloride solution is slowly added in drops, the cold bath is removed, and it is stirred vigorously for thirty minutes. After extraction with diethyl ether, the combined organic extracts are treated as usual with water and brine. After the solvent is spun off, the residue is chromatographed on silica gel (mobile solvent: ethyl acetate/hexane). 21.4 g (84.2%) of the desired compound (slightly contaminated) is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659297B2
Source datasetuspto-grants-2010_02
ORD IDord-39e973a6bd87490f99b6147ca03e361e
Source noteuspto-grants-2010_02