HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1483175Generated: October 31, 2026
Triphenylphosphine → HCID 71601674, compound
https://huagongshe.com/reaction/1483175
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | HCID 71601673 | HCID 71601673 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71601674 | HCID 71601674 | 93.2% |
Reaction Steps
Compound 27c (4.8 g, 20 mmol) was dissolved in tetrahydrofuran (10 mL). Under the protection of argon, PPh3 (5.8 g, 22 mmol) was added, and the reaction mixture was heated to 45° C. to react for 2 hrs. Then water (7.86 mL) was added and the mixture was cooled to room temperature to react for 13 hrs. TLC (dichloromethane/methanol=20/1) was employed to monitor the reaction. After the reaction completed, the mixture was diluted with water, and extracted with ethyl acetate. The organic phase was combined, washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, and then dried by rotary evaporation. Column chromatography afforded 4.0 g of white solid (compound 27d), yield 93.2%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09416144B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-bc46325822c84a9bad750e746ff2c551 |
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| Source note | uspto-grants-2016_08 |
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