HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703273Generated: October 25, 2026
Triethylamine → (2S,3R)-methyl-2-benzamidomethyl-3-hydroxybutyrate
https://huagongshe.com/reaction/703273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 2-((benzoylamino)methyl)-3-oxobutanoate | HCID 11831808 | — |
| Catalyst | Ruthenium | HCID 23950 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S,3R)-methyl-2-benzamidomethyl-3-hydroxybutyrate | HCID 10060699 | 90% |
Reaction Steps
In a 100 ml-volume stainless steel-made autoclave whose atmosphere had been displaced with nitrogen was charged a solution of 2.5 g (10 mmole) of methyl 2-(N-benzoylamino)methyl-3-oxobutanoate and 84.5 mg (0.05 mmole) of the ruthenium-optically active phosphine complex as synthesized in Reference Example 1 [Ru2Cl4 ((+)-BINAP)2 (NEt3)] in 17.5 ml of methylene chloride, and the mixture was stirred at 50° C. under a hydrogen pressure of 100 kg/cm2 for 20 hours to conduct a hydrogenation reaction. The solvent was removed from the reaction mixture by distillation, and the residue was purified by silica gel column chromatography using a mixed solvent of n-hexane and ethyl acetate as an eluent to obtain 2.25 g (yield: 90%) of methyl (2S, 3R)-2-(N-benzoylamino)methyl-3-hydroxybutanoate having an optical purity of 98 %ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04981992 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-4b5c6a4e5cd14134b423e998d4fef81d |
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| Source note | uspto-grants-1991_01 |
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