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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209714Generated: October 26, 2026

Heptane → methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate

https://huagongshe.com/reaction/2209714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptaneHCID 8900—
ReactantThionyl ChlorideHCID 24386—
ReactantN-[4-methoxybenzenesulfonyl]-(D)-valineHCID 1133588—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Productmethyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoateHCID 10946547—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of N-[4-methoxybenzenesulfonyl]-(D)-valine (8369 g, 29.13 mol) in methanol (30 L) at 5° C. is added thionyl chloride (2176 mL, 29.7 mol) over 2.5 hours. After stirring for 3 hours at 5° C., the reaction is stirred for 36 hours at room temperature. Most of the solvent is evaporated, and the chide product is dissolved in toluene (80 L). The toluene layer is then washed with water (20 L), saturated sodium bicarbonate (20 L), water again (20 L), 2N hydrochloric acid (20 L), brine (20 L), dried (Na2SO4), and the solvent is evaporated. The solid obtained is dissolved in ethyl acetate (8 L) and heptane (16 L) is added to induce crystallization. The precipitated product is collected by filtration to provide methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05455258
Source datasetuspto-grants-1995_10
ORD IDord-1af787fbae9e4395888bd102c6fccb6f
Source noteuspto-grants-1995_10