HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269630Generated: October 30, 2026
Citric Acid → (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acid
https://huagongshe.com/reaction/2269630
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-[tert-butoxycarbonyl]-L-serine | HCID 98766 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acid | HCID 7016354 | — |
Reaction Steps
In a DMF solution containing 2.00 g of Boc-Ser-OH, 0.86 g of sodium hydride (60% oily suspension) was added under ice cooling and the resultant mixture was stirred for 30 min. To the resultant solution, 0.72 ml of methyl iodide was added and the resultant solution was stirred for 3 hr. The reaction mixture was neutralized with citric acid and evaporated under reduced pressure. The obtained residue was redissolved in ethyl acetate, and the solution was washed with 5% aqueous citric acid solution and saturated aqueous sodium chloride solution, successively, and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure. The residue was subjected to a silica gel column chromatography (chloroform:methanol=10:1) and crystallized as its DCHA salt from n-hexane to give 0.79 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06329502B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-c7e583b5117847ff8d0d6168ff54b183 |
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| Source note | uspto-grants-2001_12 |
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