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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249570Generated: October 25, 2026

Propargyl bromide → 1-(1-Propylcyclobutyl)but-3-yn-1-ol

https://huagongshe.com/reaction/2249570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl bromideHCID 7842—
ReactantMagnesiumHCID 5462224—
Reactant1-Propylcyclobutane-1-carbaldehydeHCID 14301356—
SolventDiethyl EtherHCID 3283—
Product1-(1-Propylcyclobutyl)but-3-yn-1-olHCID 14254776250.6%

Reaction Conditions

Temperature40 °C

Reaction Steps

Propargyl bromide (0.27 mL, 2.4 mmol) was added to a mixture of magnesium (1.1 g, 45 mmol) and mercuric chloride (30 mg, 0.117 mmol) in Et2O (60 mL). The mixture was warmed to 40° C. until bubbling commenced. The remainder of the propargyl bromide (2.1 mL, 19 mmol) was added in small portions. After −1.5 h the reaction became cloudy white. A solution of the aldehyde 3 (0.8 g, 7 mmol) in Et2O (4 mL) was added and the reaction was stirred for 16 h. The reaction was then quenched by cautiously adding saturated aqueous NH4Cl. The resultant mixture was extracted with Et2O. The organic portion was washed with brine, dried (MgSO4), filtered and concentrated in vacuo. FCC (silica gel, 1:1 pentane/CH2Cl2) gave 1.0 g (94%) of the alcohol 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314890B2
Source datasetuspto-grants-2008_01
ORD IDord-81a15a3e8ff14f9bb438663efb15bd24
Source noteuspto-grants-2008_01