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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766918Generated: November 1, 2026

Sulfuric Acid → 2-[[Bis(allyloxy)phosphoryl]oxymethyl]-3-methylbenzoic acid

https://huagongshe.com/reaction/1766918

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantIsopropanolHCID 3776—
ReactantDiallyl 2-(hydroxymethyl)-6-methylbenzyl phosphateHCID 17862639—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-[[Bis(allyloxy)phosphoryl]oxymethyl]-3-methylbenzoic acidHCID 1786249471%

Reaction Steps

A solution of diallyl 2-(hydroxymethyl)-6-methylbenzyl phosphate (1.22 g, 4.02 mmol) obtained from Example 22-(4) 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; 6 ml, ca. 16 mmol) was added thereto. The reaction mixture was stirred at room temperature for 2 hours, and then 2-propanol (1 ml) was added thereto to stop the reaction. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure to give an oily residue. The residue was dried using a vaccum pump, and then subjected to chromatography on a silica gel (50 g) column (eluent; ethyl acetate:dichloromethane=1:1) to afford the title compound (905.3 mg, 71% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230023B2
Source datasetuspto-grants-2007_06
ORD IDord-f0a6ff0fb27b453abe6355ef68f2adcc
Source noteuspto-grants-2007_06