HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766931Generated: October 26, 2026
Sulfuric Acid → 2-[[Bis(allyloxy)phosphoryl]oxymethyl]-3-chlorobenzoic acid
https://huagongshe.com/reaction/1766931
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Diallyl 2-chloro-6-(hydroxymethyl)benzyl phosphate | HCID 17862563 | — |
| Reactant | Jones' reagent | HCID 131709961 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[[Bis(allyloxy)phosphoryl]oxymethyl]-3-chlorobenzoic acid | HCID 17862556 | 76% |
Reaction Steps
A solution of diallyl 2-chloro-6-(hydroxymethyl)benzyl phosphate (2.62 g, 7.88 mmol) obtained from Example 27-(3) in acetone (25 ml) was cooled to 0° C., and Jones reagent (a mixture of chromic anhydride (5.34 g) and concentrated sulfuric acid (4.6 ml) diluted with water to 20 ml total volume; 12 ml, ca. 32 mmol) was added thereto. The reaction mixture was stirred at room temperature for 1 hour, and then 2-propanol (1 ml) was added thereto to stop the reaction. The insoluble material was filtered off, and then the filtrate was concentrated under reduced pressure to give an oily residue. The residue was thoroughly dried using a vaccum pump, and then subjected to chromatography on a silica gel (40 g) column (eluent; ethyl acetate:dichloromethane=1:10˜1:1) to afford the title compound (2.065 g, 76% yield) as a pale brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07230023B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-f8a8e422ee3149f6885e54df0e041c4a |
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| Source note | uspto-grants-2007_06 |
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