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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl [chloro(4-chlorophenyl)methyl]phosphonate | HCID 12881548 | — |
| Reactant | 2-(5-Formylthien-2-ylethynyl)benzothiophene | HCID 19981413 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[5-(4-Chlorophenylethynyl)thien-2-ylethynyl]benzothiophene | HCID 19981414 | 19.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05073564 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-e6ff885b78e642bc83fdfeade4a57314 |
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| Source note | uspto-grants-1991_12 |
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