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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647088Generated: October 31, 2026

Allyl bromide → HCID 57291064, compound

https://huagongshe.com/reaction/647088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 13282982HCID 13282982—
SolventWaterHCID 962—
ProductHCID 57291064HCID 57291064—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 250 ml single neck round bottom flask equipped with a reflux condensor and an argon inlet is added 2.35 gm of the 3-pyridyl-1-naphthylcarbinol and 100 ml of anhydrous tetrahydrofuran. The system is cooled to 0° C. and after cooling 0.26 gm sodium hydride is added. The system is stirred for an additional 20 minutes and 1.1 ml of allyl bromide is added. The system is allowed to come to room temperature over 1/2-hour and is stirred there for an additional 2 hours. Afterwards, the system is heated at reflux for 17 hours. At this time, water is added to the system and the product extracted with methylene chloride. The methylene chloride is then washed with water and dried over sodium sulfate. The methylene chloride is removed by stripping to give the 3-pyridyl-1-naphthylcarbinol allylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04407806
Source datasetuspto-grants-1983_10
ORD IDord-bb9d3332241f4f2aa4bfac033b771542
Source noteuspto-grants-1983_10