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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212324Generated: November 3, 2026

Propargyl alcohol → Methyl 3,5-bis-(3-hydroxyprop-1-ynyl)benzoate

https://huagongshe.com/reaction/2212324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropargyl alcoholHCID 7859—
ReactantTert-butyl 3,5-dibromobenzoateHCID 21964570—
CatalystHCID 178418397HCID 178418397—
SolventTriethylamineHCID 8471—
ProductMethyl 3,5-bis-(3-hydroxyprop-1-ynyl)benzoateHCID 21964565101.9%

Reaction Steps

Pd(Ph3P)4 (1.08 g), CuBrSMe2 (0.41 g) and propargyl alcohol (2.95 g, 50.2 mmol) are added successively to a solution of methyl 3,5-dibromobenzoate (A6, 7.7 g, 22.9 mmol) in triethylamine (130 ml), and the mixture is stirred at RT for 10 min and then under reflux at 80° C. for 3.5 h. After cooling, the reaction mixture is filtered off with suction through kieselguhr, and the filter cake is washed with ethyl acetate (50 ml). The organic phase is concentrated under reduced pressure. Further purification is carried out by chromatography [toluene/acetone (8:2)] on a silica gel column. This gives the title compound (5.7 g) as a colorless solid. TLC, silica gel (glass plates), [toluene/acetone (7.5:2.5)], Rf=0.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101911B2
Source datasetuspto-grants-2006_09
ORD IDord-d998a1ca5faf4a27a9121acad545c0e5
Source noteuspto-grants-2006_09