HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591418Generated: November 1, 2026
Phosphorus oxychloride → HCID 9925643, compound
https://huagongshe.com/reaction/1591418
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 135532690 | HCID 135532690 | — |
| Catalyst | N,N-Diethylaniline | HCID 7061 | — |
| Product | HCID 9925643 | HCID 9925643 | 72% |
Reaction Steps
The title compound of Example 23 (10.0 g, 38.37 mmol) was heated to reflux in phosphorus oxychloride (200 ml) and N,N-diethylaniline (3-4 drops) for 5 hours under nitrogen. The solution was then cooled to room temperature, concentrated to dryness, and the syrup was dissolved in cold (~ -10° C.) methylene chloride (200 ml). The organic layer was treated with saturated aqueous sodium bicarbonate (100 ml) with vigorous stirring, and the temperature was kept below 5° C. as solid sodium bicarbonate was added portionwise to elevate the pH to between 5 and 7. The layers were separated and the aqueous phase was extracted with methylene chloride. The combined organic layers were filtered over phase-separator paper, concentrated and dried under vacuum to give the title compound (7.71 g, 72%) as a yellow-white solid sufficiently pure to employ in the next step. Recrystallisation of the solid from hexane/methylene chloride provided an analytical sample, m.p. 166°-169° C.; 'H-NMR (DMSO-d6) δ 1.09 (d, J=6.9 Hz, 6H, (CH3)2CH), 2.79 m, J=6.9 Hz, 1H, (CH3)2CH), 11.61 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05206435 |
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| Source dataset | uspto-grants-1993_04 |
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| ORD ID | ord-31479497dec24408945b290f31f1a4f7 |
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| Source note | uspto-grants-1993_04 |
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