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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455006Generated: October 31, 2026

Allyl Alcohol → HCID 86602453, compound

https://huagongshe.com/reaction/1455006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl AlcoholHCID 7858—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86602451HCID 86602451—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventTolueneHCID 1140—
ProductHCID 86602453HCID 86602453—

Reaction Steps

To the subtitle product of step ii) (1.0 g) in toluene was added allyl alcohol (0.23 g), sodium hydroxide (0.16 g) and benzyltriethylammonium chloride (10 mg). The mixture was stirred at room temperature for 2 h before sodium hydroxide solution (10 ml, 1M) was added the organics extracted with EtOAc (2×50 ml). The combined organics were washed with brine (20 ml) and dried (MgSO4). The solid was filtered and the filtrate evaporated to dryness to yield the subtitle compound as a white solid. Yield 1.0 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07482355B2
Source datasetuspto-grants-2009_01
ORD IDord-0ced63389f194c8cb292e60530212048
Source noteuspto-grants-2009_01