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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dimethyl 2-methoxymethylbenzylphosphonate | HCID 19937177 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethylphosphono-(2-methoxymethylphenyl)-acetic acid | HCID 19937251 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05416068 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-acc2a54f37d442768b4ca50eac77a62d |
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| Source note | uspto-grants-1995_05 |
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