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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902677Generated: October 27, 2026

Hydrochloric Acid → 2-(Thiophen-3-yl)propanal

https://huagongshe.com/reaction/902677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantThiopheneHCID 8030—
Product2-(Thiophen-3-yl)propanalHCID 1247728130%

Reaction Steps

A solution of methoxymethyldiphenyl phosphonium chloride (4 g, 11.9 mmol) in anhydrous ethanol (50 ml) was cooled to 0° C. and sodium ethoxide (0.8 g, 8.25 mmol) was added. After the mixture had warmed to room temperature, 1-thiophen-3-yl-ethanone (0.7 g, 5.9 mmol) was added and the reaction mixture was heated to 120° C. for 30 min in Microwave. The mixture was filtered and the filtrate was concentrated. The crude product was purified by silica gel column chromatograph using EtOAc:Hexane/20:80 as the eluent to give 0.5 g (54.5% yield) 3-((E or Z)-2-methoxy-1-methyl-vinyl)-thiophene. The solution of 3-((E or Z)-2-methoxy-1-methyl-vinyl)-thiophene in THF:HCl: H2O (10 ml total, 9:0.5:1) was heated to 150° C. for 30 min in microwave. After the mixture was concentrated the residue was partitioned between EtOAc and water. The combined organic layers were washed with sodium bicarbonate, water, brine, dried over sodium sulfate and concentrated to give the title compound as an oil 250 mg (30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365085B2
Source datasetuspto-grants-2008_04
ORD IDord-824c8b03be5f428a9c6b40304b97e3ff
Source noteuspto-grants-2008_04