Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269652Generated: October 29, 2026

Methyl iodide → (2S,3R)-2-{[(tert-butoxy)carbonyl]amino}-3-methoxybutanoic acid

https://huagongshe.com/reaction/2269652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantN-tert-Butoxycarbonyl-L-threonineHCID 2724766—
SolventTetrahydrofuranHCID 8028—
Product(2S,3R)-2-{[(tert-butoxy)carbonyl]amino}-3-methoxybutanoic acidHCID 15460346—

Reaction Steps

In a THF solution containing 0.8 g of Boc-Thr-OH, 100 mg of sodium hydride (60% in oil) was added under ice cooling and the resultant mixture was stirred for 30 min at room temperature. Further, 2.8 ml of methyl iodide was added and the obtained reaction mixture was stirred overnight at room temperature. The reaction mixture was evaporated under reduced pressure and the resultant residue was redissolved in ethyl acetate, washed with 5% sodium hydrogensulfite aqueous solution, water and saturated sodium chloride aqueous solution, successively, and dried over anhydrous sodium sulfate. The dried solution was evaporated under reduced pressure, dissolved in methanol, mixed with DCHA and reevaporated. Ether-hexane was added to the residue to give 0.55 g of the title compound as its DCHA salt.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329502B1
Source datasetuspto-grants-2001_12
ORD IDord-483e46cf61b245a5b5bdde046e4289ca
Source noteuspto-grants-2001_12