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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantN-[tert-butoxycarbonyl]-L-serineHCID 98766—
SolventDimethylformamideHCID 6228—
Product(2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329502B1
Source datasetuspto-grants-2001_12
ORD IDord-c7e583b5117847ff8d0d6168ff54b183
Source noteuspto-grants-2001_12