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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333432Generated: October 30, 2026

1-Bromopentane → 2-Phenylheptanenitrile

https://huagongshe.com/reaction/333432

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopentaneHCID 8057—
ReactantPhenylacetonitrileHCID 8794—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product2-PhenylheptanenitrileHCID 1265202064%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 2 g of 60% NaH in 50 mL of DMF cooled to 0° C. are added dropwise 5 g (42.7 mmol) of phenylacetonitrile. After stirring for 30 minutes at 0° C., 5.32 mL (42.7 mmol) of bromopentane are added dropwise. The reaction medium is stirred for 16 hours at room temperature and then treated with ice and extracted with ethyl ether. The organic phase is washed with saturated aqueous sodium hydrogen carbonate solution, dried over sodium sulfate, filtered and evaporated under pressure. An orange-yellow oil is obtained and purified by fractional distillation under reduced pressure (70-75° C. at 1×10−1 mbar). 5.14 g in the form of an orange-coloured oil are obtained in a yield of 64%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877968B2
Source datasetuspto-grants-2014_11
ORD IDord-b8c699b5bac942dfa635d89a2552b483
Source noteuspto-grants-2014_11