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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604426Generated: November 2, 2026

Methyl iodide → (+/-)-3-(Cyclopentyloxy)-4-methoxy-alpha-methylbenzeneacetonitrile

https://huagongshe.com/reaction/1604426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant3-(Cyclopentyloxy)-4-methoxyphenylacetonitrileHCID 10728228—
ReactantLithium diisopropylamineHCID 45051747—
SolventTetrahydrofuranHCID 8028—
Product(+/-)-3-(Cyclopentyloxy)-4-methoxy-alpha-methylbenzeneacetonitrileHCID 22456815100%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of 3-(cylcopentyloxy)-4-methoxybenzeneacetonitrile (20 g) in THF (200 ml) was stirred at -78° C. under a N2 flow. N-(1-methylethyl)-2-propanamine lithium salt (45 ml) was added dropwise and the resulting mixture was stirred for 30 minutes at -78° C. Iodomethane (13.5 g) was added dropwise and the resulting reaction mixture was allowed to warm to RT. The reaction mixture was stirred for 2 hours. The mixture was quenched with a saturated aqueous NH4Cl solution (200 ml) and was extracted with CH2Cl2 (3×φml). The separated organic layer was dried (MgSO4), filtered and the solvent was evaporated, yielding 17.7 g (100%) of (±)-3-(cyclopentyloxy)-4-methoxy-α-methylbenzeneacetonitrile (interm. 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994376
Source datasetuspto-grants-1999_11
ORD IDord-8b78e3eed0174b4fa02bacb28dbd6090
Source noteuspto-grants-1999_11