HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647224Generated: November 1, 2026
4'-Fluoroacetophenone → HCID 54261868, compound
https://huagongshe.com/reaction/1647224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4'-Fluoroacetophenone | HCID 9828 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | m-Formylbenzonitrile | HCID 90670 | — |
| Reactant | Dimethyl diphenylsilane | HCID 136618 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54261868 | HCID 54261868 | 41.8% |
Reaction Steps
Triflic acid (3.2 g, 21 mmol) is added portionwise to diphenyldimethylsilane (2.22 g, 10.5 mmol) in 20 mL of dichloromethane and stirred for 1 hour. After cooling to -78° C., diisopropylethylamine (1.42 g, 11 mmol) and 4'-fluoroacetophenone (1.38 g, 10 mmol) are added and the reaction mixture stirred for another hour before adding 3-cyanobenzaldehyde (1.0 g, 7.62 mmol). After the reaction mixture is stirred 18 hours, it is diluted with 100 mL of dichloromethane and stirred 1 hour with a saturated solution of sodium bicarbonate. The organic layer is separated, dried (MgSO4), concentrated and columned over SiO2 eluting with dichloromethane to provide 0.8 g of the title compound; mp 170°-172° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05430047 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-1747380f47dd41559cd956c6854adc21 |
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| Source note | uspto-grants-1995_07 |
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