Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36607Generated: October 28, 2026

Carbon Dioxide → Dimethylphosphono-(2-methoxymethylphenyl)-acetic acid

https://huagongshe.com/reaction/36607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantDiethyl EtherHCID 3283—
ReactantDimethyl 2-methoxymethylbenzylphosphonateHCID 19937177—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductDimethylphosphono-(2-methoxymethylphenyl)-acetic acidHCID 19937251—

Reaction Conditions

Temperature20 °C

Reaction Steps

165 ml of a 1.6 M solution of n-butyllithium in hexane was added at (-65)° C. to 170 ml of absolute tetrahydrofuran. At this temperature a solution of 61 g of dimethyl 2-methoxymethylbenzylphosphonate (from Example 8) in 100 ml of tetrahydrofuran was dripped in. After 30 minutes the batch was poured into a (-60)° C. cold saturated solution (500 ml) of dry ice and diethyl ether. After the batch had been stirred for 10 minutes it was allowed to heat up to about 20° C. over a period of 4 hours. 300 ml of water was added and the organic phase was separated off and extracted three times, each time with 100 ml of 100 ml of 10% strength sodium carbonate solution. The combined aqueous phases were extracted twice, each time with 150 ml of diethyl ether, and the pH was adjusted to 1 with 2 N sulfuric acid. Extraction was carried out three times, each time with 150 m]of dichloromethane, the organic phases were dried, and the solvent was removed under reduced pressure. There remained 60 g of dimethylphosphone-(2-methoxymethylphenyl)-acetic acid as a yellow

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05416068
Source datasetuspto-grants-1995_05
ORD IDord-acc2a54f37d442768b4ca50eac77a62d
Source noteuspto-grants-1995_05