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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453422Generated: October 30, 2026

Methyl iodide → (R)-2-(1-methoxy-4-methylpentan-2-yl)isoindoline-1,3-dione

https://huagongshe.com/reaction/1453422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexamethylphosphoramideHCID 12679—
ReactantSodium hydrideHCID 24758—
Reactant(R)-2-(1-hydroxy-4-methylpentan-2-yl)isoindoline-1,3-dioneHCID 66772663—
SolventTetrahydrofuranHCID 8028—
Product(R)-2-(1-methoxy-4-methylpentan-2-yl)isoindoline-1,3-dioneHCID 66772667—

Reaction Steps

(R)-2-(1-hydroxy-4-methylpentan-2-yl)isoindoline-1,3-dione (example 9c) (5.88 g, 23.87 mmol) was dissolved in dry THF (25 mL) and hexamethyl-phosphoramide (30 mL) and the solution cooled to 0° C. Sodium hydride (60% in mineral oil, 1.15 g, 28.65 mmol) was added and after 10 minutes iodomethane (7.43 ml, 119.35 mmol) was added dropwise and the solution was warmed up slowly to room temperature and stirred over night. The reaction mixture was poured into ice/water, extracted with EtOAC, washed with brine, dried over MgSO4, filtered and evaporated. The residue was purified on silica gel (20% EtOAC in hexane) to give 3.92 g of (R)-2-(1-methoxy-4-methylpentan-2-yl)isoindoine-1,3-dione (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476399B2
Source datasetuspto-grants-2009_01
ORD IDord-60f58a9784aa4c339c48cdf55370fb0e
Source noteuspto-grants-2009_01