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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840352Generated: October 29, 2026

Dimethylformamide → HCID 59918716, compound

https://huagongshe.com/reaction/840352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTrimethyl orthoformateHCID 9005—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ReactantHCID 15198452HCID 15198452—
SolventBenzeneHCID 241—
ProductHCID 59918716HCID 5991871697%

Reaction Steps

Preparation of the title compound was conducted on a larger scale as follows. [R-(R*,S*)]-β-(Benzoylamino)-α-hydroxybenzenepropanoic acid, ethyl ester (3.138 g) was suspended in benzene (100 ml), and trimethoxymethane (3.190 g) and PPTS (628 mg) were added. The reaction solution was heated to reflux, 20 ml of DMF were added for dissolution of most of the starting compound, followed by heating with a Soxhlet extractor. The thimble in the extractor was filled with 4 Å mol. sieves. After 1 hour, and approximately 3 to 4 cycles in the Soxhlet extractor, TLC showed consumption of the starting material, and a new major spot of the title product. It was diluted with EtOAc, washed with NaHCO3 and H2O, dried and the solvent removed. NMR showed the presence of the title product and a small impurity. The product was purified on HPLC (hexane:ethyl acetate, 3:1) to give 3.138 g (97%) of the title product. The product (an oil) was a mixture of diastereomers (not separated). Mass spec.: M+H+=356

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365750B1
Source datasetuspto-grants-2002_04
ORD IDord-528bb5f0cdd14d93bbe13205ee61d5d6
Source noteuspto-grants-2002_04