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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantIsopropanolHCID 3776—
ReactantDiallyl 2-chloro-6-(hydroxymethyl)benzyl phosphateHCID 17862563—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-[[Bis(allyloxy)phosphoryl]oxymethyl]-3-chlorobenzoic acidHCID 1786255676%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230023B2
Source datasetuspto-grants-2007_06
ORD IDord-f8a8e422ee3149f6885e54df0e041c4a
Source noteuspto-grants-2007_06