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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2078076Generated: October 30, 2026

Bis(2-bromoethyl) ether → 4-(3-Methoxyphenyl)oxane-4-carbonitrile

https://huagongshe.com/reaction/2078076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-bromoethyl) etherHCID 21521—
ReactantSodium hydrideHCID 24758—
Reactant(3-Methoxyphenyl)acetonitrileHCID 88310—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-(3-Methoxyphenyl)oxane-4-carbonitrileHCID 1878636693.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of NaH (3.2 g, 79 mmol) in 50 mL NMP stirred at 0° C., was treated dropwise with a mixture of 2-(3-methoxyphenyl)acetonitrile (3.9 g, 26 mmol) and 1-bromo-2-(2-bromoethoxy)ethane (6.1 g, 26 mmol) in 20 mL. The mixture was allowed to warm to room temperature and stirred for 15 hours, M+1=218. The mixture was then carefully quenched with 100 mL H2O and the pH was adjusted to 5. The mixture was extracted with ether (3×100 mL). The combined organic layers were washed with H2O (3×50 mL) and brine (20 mL). The organic layer was dried over anhydrous Na2SO4, concentrated in vacuo, and purified by column chromatography eluting with 10-20% EtOAc/hexane to give 5.28 g of the crude product 5.28 g as a pale yellow oil. MS (m/z)=218 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07928139B2
Source datasetuspto-grants-2011_04
ORD IDord-f707ba80e5d44ea3b08ba8d6bf0f9887
Source noteuspto-grants-2011_04