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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 61437Generated: October 25, 2026

Water → 1-benzyl 4-methyl (2S)-2-[benzyl((2S)-2-hydroxy-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinate

https://huagongshe.com/reaction/61437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium FluorideHCID 5235—
ReactantOxiranemethanol, 4-methylbenzenesulfonate, (S)-HCID 153296—
ReactantTrimethylaluminumHCID 16682925—
ReactantAcetone cardiceHCID 18522661—
Reactant(S)-2-benzylamino-succinic acid 1-benzyl ester 4-methyl esterHCID 67303755—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
Product1-benzyl 4-methyl (2S)-2-[benzyl((2S)-2-hydroxy-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinateHCID 8734866891.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of (2S)-(+)-glycidyl tosylate (23.0 g, 0.101 mol) in 500 mL of methylene chloride was added 2.00 M of trimethylaluminum in toluene (50.4 mL) at −78 Celsius, under an atmosphere of nitrogen. After stirred at −78 Celsius for 10 min, to the mixture was added a solution of (S)-2-benzylamino-succinic acid 1-benzyl ester 4-methyl ester (30.0 g, 0.0916 mol) in 150 mL of methylene chloride. The resulting reaction mixture was stirred at −78 Celsius for 30 min. The dry ice-acetone bath was changed to an ice-water bath to warm the mixture up to 0 Celsius. The mixture was stirred at 0 Celsius for 30 min. To the reaction mixture was added sodium fluoride (16.2 g, 0.385 mol) followed by water (10.4 mL, 0.577 mol) at 0 Celsius. The resulting suspension was rapidly stirred for 1 h at 0 Celsius and filtered through a short column of of celite and the column was subsequently washed with 600 mL of methylene chloride. The combined filtrates were dried over sodium sulfate, concentrated to dry and purified by column purification (eluting with 0 to 20% EtOAc in hexane) to yield The titled compound (46.7 g, 91.7%). MS (ESI): (M+H)+=556.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440958B2
Source datasetuspto-grants-2016_09
ORD IDord-7c89de2946d546558751170c624ed971
Source noteuspto-grants-2016_09