HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437531Generated: October 27, 2026
Acetic Acid → N-[1-(Diphenylphosphoryl)butyl]urea
https://huagongshe.com/reaction/437531
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Butanal | HCID 261 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Ethyl diphenylphosphinite | HCID 69754 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | N-[1-(Diphenylphosphoryl)butyl]urea | HCID 21423533 | 33.5% |
Reaction Steps
When a mixture of 0.50 mole of ethyl diphenylphosphinite, 0.55 mole of n-butyraldehyde, and 0.25 mole of urea in 150 ml of chlorobenzene is warmed at 110° C for 3 hr, there is only a slow reaction. The mixture is cooled to room temperature and 0.25 mole of acetic acid is addded dropwise in ~10 minutes. The temperature increases to 65° during this addition; the urea dissolves and then a white solid product separates. The addition of another 0.25 mole of acetic acid causes no additional heat of reaction. The reaction mixture is warmed at 65°-80° for 9.5 hr and filtered, giving 44.4g. Recrystallization from ethylene glycol gives 26.5g of a white solid: mp 241°-244°; 31P nmr (CF3CO2H) -44.4 ppm; ms M+ = 316 (theory 316).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04031170 |
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| Source dataset | uspto-grants-1977_06 |
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| ORD ID | ord-cfd1eb6a1ba74c039c92eb62da3219a4 |
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| Source note | uspto-grants-1977_06 |
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