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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006087Generated: October 31, 2026

Hydrochloric Acid → 2(R)-(4-methoxy-2,3,6-trimethylbenzenesulfonylamino)-3-methylbutyric acid benzyl ester

https://huagongshe.com/reaction/1006087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant4-Methoxy-2,3,6-trimethylbenzenesulfonyl chlorideHCID 562787—
ReactantBenzyl D-valinateHCID 7350007—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2(R)-(4-methoxy-2,3,6-trimethylbenzenesulfonylamino)-3-methylbutyric acid benzyl esterHCID 1148693298.8%

Reaction Steps

To a solution of D-valine benzyl ester (4 g, 19.3 mmol) and trimethylsilylcyanide (7.2 mL, 57.9 mmol) in acetonitrile (40 mL) was added 4-methoxy-2,3,6-trimethylbenzenesulfonyl chloride (4.8 g, 19.3 mmol). After 3 h, the reaction mixture was diluted with ethyl acetate (100 mL) and transferred to a separatory funnel. Aqueous hydrochloric acid (120 mL, 2.5%) was added and the organic layer was separated and washed with 5% sodium bicarbonate and brine and then dried over magnesium sulfate. The organics were removed in vacuo to give 2(R)-(4-methoxy-2,3,6-trimethylbenzenesulfonylamino)-3-methylbutyric acid benzyl ester (8 g) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06787559B2
Source datasetuspto-grants-2004_09
ORD IDord-51948b229640491b9238fc987a19bf8e
Source noteuspto-grants-2004_09