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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649483Generated: November 4, 2026

Allyl bromide → HCID 131713234, compound

https://huagongshe.com/reaction/1649483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
ReactantHCID 70523198HCID 70523198—
SolventWaterHCID 962—
ProductHCID 131713234HCID 131713234—

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 5-pyrimidyl-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 5-pyrimidyl-1-naphthylcarbinol allylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04417050
Source datasetuspto-grants-1983_11
ORD IDord-63270df18e474d5892bff007a47c3294
Source noteuspto-grants-1983_11