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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444495Generated: October 31, 2026

Ammonium Chloride → HCID 17989149, compound

https://huagongshe.com/reaction/1444495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant2-(Benzenesulfonyl)-3-phenyloxaziridineHCID 320405—
ReactantHCID 17989120HCID 17989120—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 17989149HCID 1798914984.2%

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 1¾ hours, 236.9 ml of a 0;5 molar solution of potassium-bis-(trimethylsilylamide) in toluene is added in drops, and the reaction mixture then is 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 vigorously stirred for 30 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 is isolated (easily contaminated).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662821B2
Source datasetuspto-grants-2010_02
ORD IDord-1ef54f9cbd2b4013ae732a355210d6fd
Source noteuspto-grants-2010_02