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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588928Generated: November 2, 2026

Tetrahydrofuran → HCID 67874296, compound

https://huagongshe.com/reaction/1588928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—
ReactantHCID 54488742HCID 54488742—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventEther tetrahydrofuranHCID 21868444—
ProductHCID 67874296HCID 67874296—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a stirred solution of 4-bromo-1,2-(methylenedioxy)benzene (1.00 g, 6.0 mmol) in ethyl ether (30 mL) at 0° under an argon atmosphere is added n-BuLi (3.75 mL of 1.6 M solution in hexane). Tetrahydrofuran (10 mL) is added. The reaction mixture is cooled to -20° C. and a solution of terephthalaldehydic acid N-isopropyl-N-cyclohexyl amide (0.82 g, 3.0 mmol) in THF: ethyl ether (4:3, 35 mL) is added rapidly. The reaction is followed by thin layer chromatography until complete. The reaction is quenched at -15° C. by adding water (50 mL) and 1N HCl(20 mL). The reaction is further diluted with water (300 mL) and extracted three times with EtOAc (50 mL portions). The combined extracts are washed twice with saturated NaCl solution and dried (MgSO4). The drying agent is filtered and the filtrate concentrated in vacuo to give the crude product. The crude product is chromatographed on silica gel using mixtures of ethyl acetate and hexane as eluents to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05223539
Source datasetuspto-grants-1993_06
ORD IDord-f9040b49b3d442c8871f1ec40661e79c
Source noteuspto-grants-1993_06