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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460994Generated: November 2, 2026

Diethyl [chloro(4-chlorophenyl)methyl]phosphonate → 2-[5-(4-Chlorophenylethynyl)thien-2-ylethynyl]benzothiophene

https://huagongshe.com/reaction/1460994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl [chloro(4-chlorophenyl)methyl]phosphonateHCID 12881548—
Reactant2-(5-Formylthien-2-ylethynyl)benzothiopheneHCID 19981413—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethylformamideHCID 6228—
Product2-[5-(4-Chlorophenylethynyl)thien-2-ylethynyl]benzothiopheneHCID 1998141419.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of 0.75 gram (0.0028 mole) of 2-(5-formylthien-2-ylethynyl)benzothiophene and 0.83 gram (0.0028 mole) of diethyl (4-chlorophenyl)chloromethylphosphonate in 10 ml of dimethylformamide was cooled to 0° C., and 0.94 gram (0.0084 mole) of potassium tertbutoxide was added. Upon completion of addition, the reaction mixture was stirred at 0° C. for 30 minutes and then was allowed to warm to ambient temperature where it was stirred for 18 hours. After this time the reaction mixture was subjected to column chromatography on silica gel. Elution was accomplished using hexane. The appropriate fractions were combined and concentrated under reduced pressure, yielding 0.20 gram of 2-[5-(4-chlorophenylethynyl)thien-2-ylethynyl]benzothiophene; m.p. 189°-191° C. The nmr spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05073564
Source datasetuspto-grants-1991_12
ORD IDord-e6ff885b78e642bc83fdfeade4a57314
Source noteuspto-grants-1991_12