참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | O-Xylene | HCID 7237 | — |
| 반응물 | Benzal chloride | HCID 7411 | — |
| 반응물 | Diethylphosphite | HCID 3780918 | — |
| 반응물 | Sodium | HCID 5360545 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | RU78783 | HCID 447537 | — |
반응 단계
There were charged into the reaction vessel 23.0 grams (1.0 mole) of sodium metal along with 90 cc. of xylene and 80 cc. of tetrahydrofurane. The vessel was placed under a nitrogen blanket and 138.10 grams (1.0 mole) of diethyl phosphite added over a 35 minute period. An exothermic reaction ensued which was maintained at 62° C. by external cooling. After addition was complete the mixture was heated to 100° C. and held there until all of the sodium metal was gone. The mixture was cooled to 60° to 70° C. and 80.50 grams (0.5 mole) of benzal chloride were added gradually over a 25 minute period. An exothermic reaction ensued which was maintained at 60° to 70° C. by external cooling. The mixture was then heated for 4 hours at 70° to 75° C., cooled to 60° C. The liquid material was separated from the solid and the solid boiled 8 times with 100 cc. of benzene to extract the organic material. The eluate product was then distilled, terminal conditions being a pot temperature of 201° C., distillate temperature 125° C. and pressure 6 mm. The solid residue of 70 grams was tetraethyl phenyl methane diphosphonate. This product was hydrolyzed and the hydrolysis product purified as in Example 1 to obtain phenyl methane diphosphonic acid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04440646 |
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| 출처 데이터셋 | uspto-grants-1984_04 |
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| ORD ID | ord-483e34dc895e45988dd43a0bf485fd25 |
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| 출처 메모 | uspto-grants-1984_04 |
|---|