HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644104Generated: October 30, 2026
Phosphorus oxychloride → HCID 23124897, compound
https://huagongshe.com/reaction/644104
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indole | HCID 736229 | — |
| Reactant | 60838-50-8 | HCID 5324713 | — |
| Reactant | HCID 67196878 | HCID 67196878 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23124897 | HCID 23124897 | 45% |
Reaction Steps
Into a solution prepared by dissolving 0.63 g of 3-(4-fluorophenyl)-1-isopropyl-1H-indole in 3 mL of dichloromethane was added dropwise 0.77 g of phosphorus oxychloride at an inner temperature of 0 to 10° C., then, 0.92 g of trans-3-methoxyacrylonitrile was added dropwise. Then, the mixture was stirred overnight at room temperature to cause a reaction, further, the mixture was reacted for 6 hours at the reflux temperature. After completion of the reaction, the reaction liquid was added into 100 mL of 5 wt % aqueous sodium hydrogen carbonate, and extracted with ethyl acetate three times. The resulting organic layers were combined and washed with water, then, dried with anhydrous magnesium sulfate. The magnesium sulfate was filtrated off, and the resulting filtrate was concentrated to obtain a concentrated residue containing 3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]acrylonitrile (trans-cis isomer mixture containing mainly trans isomer). The resulting concentrated residue was purified by silica gel column chromatography (developing liquid: n-heptane/ethyl acetate: 10/1 to 5/1) to obtain 0.34 g of trans-3-[3-(4-fluorophenyl)-1-isopropyl-1H-indol-2-yl]acrylonitrile (yellow solid). Yield: 45%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700642B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-82f3d86290f64b56b5e2170555f0f2bd |
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| Source note | uspto-grants-2010_04 |
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