HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275433Generated: October 31, 2026
Hexamethylphosphoramide → HCID 57292408, compound
https://huagongshe.com/reaction/275433
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 22420756 | HCID 22420756 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57292408 | HCID 57292408 | 57.5% |
Reaction Steps
A mixture of 1.02 g (4.68 mmol) of N-(4'-fluorophenyl)-3-methylglutarimide (Compound 66), 0.88 g (2.2 mmol) of 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane-2,4-disulfide (known as Lawesson's Reagent), and 6 ml of hexamethylphosphoramide in a 50 ml round-bottomed flask was warmed to 95°-100° C. for 21 hours. An additional 1.05 g (2.5 mmol) of Lawesson's Reagent were added and heating to 100° C. was continued for an additional 30 hours. The mixture was allowed to cool to room temperature and water (50 ml) was added. The mixture was extracted with ether (4×50 ml). The organic portions were combined, dried over MgSO4 and the solvent was removed in vacuo. The resulting 2 g of orange oil were purified via flash chromatography (silica gel, 1:1 hexanes/methylene chloride) to yield 300 mg (28% yield) of yellow oil which solidified to a solid: m.p. 84.5°-87.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05393735 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-7164324f17e34336840e1a850a17e91d |
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| Source note | uspto-grants-1995_02 |
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