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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807411Generated: November 1, 2026

1-(Triphenylphosphoranylidene)acetone → HCID 67086773, compound

https://huagongshe.com/reaction/1807411

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Triphenylphosphoranylidene)acetoneHCID 15038—
Reactant3-Thiophenecarboxaldehyde, 2,4,5-trichloro-HCID 173786—
CatalystLithium BromideHCID 82050—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 67086773HCID 6708677391.3%

Reaction Steps

To a stirred solution of 2,4,5-trichloro-thiophene-3-carbaldehyde (10.3 g; 48 mmol) and lithium bromide (0.10 g; 1.2 mmol) in acetonitrile (100 mL) at 15° C. under nitrogen was added acetylmethylene-triphenylphosphorane (15.6 g; 49 mmol). The reaction mixture was stirred for 3 hours at ambient temperature then poured in water (200 ml) and extracted with dichloromethane (3×70 ml). Combined organic layers were dried over anhydrous sodium sulphate. The solvent was removed in vacuo and the residue was purified by chromatography over silica gel (eluant: cyclohexane/ethyl acetate 90:10) to afford 11.2 g (91% of theory) of (E)-4-(2,4,5-trichloro-thiophen-3-yl)-but-3-en-2-one as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357635B2
Source datasetuspto-grants-2013_01
ORD IDord-411bd0ef44fe492bb8df82547a1ba29f
Source noteuspto-grants-2013_01