HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840352Generated: October 29, 2026
Dimethylformamide → HCID 59918716, compound
https://huagongshe.com/reaction/840352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Trimethyl orthoformate | HCID 9005 | — |
| Reactant | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| Reactant | HCID 15198452 | HCID 15198452 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 59918716 | HCID 59918716 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06365750B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-528bb5f0cdd14d93bbe13205ee61d5d6 |
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| Source note | uspto-grants-2002_04 |
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