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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1518774Generated: November 4, 2026

Methyl iodide → Boc-N-methyl-D-Valine

https://huagongshe.com/reaction/1518774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(2R)-2-(((tert-butoxy)carbonyl)amino)-3-methylbutanoic acidHCID 637605—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductBoc-N-methyl-D-ValineHCID 7018800100.6%

Reaction Steps

To a solution of N-Boc-D-Val-OH (1.0 g, 4.60 mmol) in THF (15.3 mL) at 0° C. was added MeI (2.88 mL, 46.0 mmol, 10.0 equiv). NaH (60%, 1.84 g, 46.0 mmol, 10.0 equiv) was added as a solid to the suspension over a period of 2 hours. After stirring for 12 hours at room temperature, the reaction mixture was diluted with diethyl ether and quenched with water slowly. Aqueous layer was extracted with diethyl ether followed by acidified to pH 3 with 10% citric acid and extraction with ethyl acetate. Combined organic layer was washed with brine, dried with Na2SO4, filtered and concentrated in vacuo to afford compound 3.3a (1.07 g) which was used for the next step without further purification. MS m/z (M+Na) 254.2. 1H NMR (400 MHz, CDCl3) 4.02-4.17 (m, 1H), 2.88 (s, 3H), 2.40-2.14 (m, 1H), 1.54-1.39 (m, 9H), 1.03 (d, J=6.60 Hz, 3H), 0.92 (d, J=6.70 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09072696B2
Source datasetuspto-grants-2015_07
ORD IDord-f411adeb265447efa36923cacea8d82d
Source noteuspto-grants-2015_07