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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683972Generated: November 1, 2026

[1-(2-Oxoethyl)cyclopropyl]acetonitrile → [1-(2-Hydroxypropyl)cyclopropyl]acetonitrile

https://huagongshe.com/reaction/1683972

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[1-(2-Oxoethyl)cyclopropyl]acetonitrileHCID 19041707—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product[1-(2-Hydroxypropyl)cyclopropyl]acetonitrileHCID 1904163772.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a -5° C. solution of the aldehyde from Step 2 (3.00 g, 24.4 mmol) in 65 mL of THF was added methyl magnesium chloride (3.0M solution in THF, 9.5 mL, 29 mmol) and the reaction was stirred 2 h at 0° C. The reaction was quenched with 1M HCl and extracted with ethyl acetate. The organic extracts were washed with saturated NaHCO3 and brine and dried over MgSO4. Purification by flash chromatography (30% ethyl acetate/hexanes) provided 2.46 g of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05639780
Source datasetuspto-grants-1997_06
ORD IDord-a7bfc9dfccc74fdd926ebaabd6a5c5b2
Source noteuspto-grants-1997_06