참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodine | HCID 807 | — |
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Phosphorus trichloride | HCID 24387 | — |
| 반응물 | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| 반응물 | Acetone cardice | HCID 18522661 | — |
| 반응물 | chloride THF | HCID 21908598 | — |
| 촉매 | Mercury dibromide | HCID 24612 | — |
| 생성물 | Tris(2-methoxyethoxymethyl)phosphine | HCID 54193331 | — |
반응 단계
To ground Mg metal (5.2 g, 214 mmol) was added I2 (1 crystal), HgBr2 (10 mg) and 2 ml of a solution of 2-methoxyethoxymethyl chloride (25 g, 201 mmol) in THF (100 ml) at R.T. After 30 sec, the reaction started and was cooled to -30° C. (dry-ice/acetone). The remaining chloride/THF solution was added dropwise at -20° to -10° C. over 2 h. The mixture was stirred at 0° C. for 2h post-addition and cooled to -78° C. The reagent was then treated with PCl3 (2.2 ml, 25.1 mmol) according to General Method I and the final residue was purified by distillation to afford 1.6 (21%) of tris(2-methoxyethoxymethyl)phosphine as a colorless mobile oil (b.p.=150°-160° [email protected] mmHg). 31P-NMR(CDCl3): -42.7. MS(LREI)m/z=299(M+1 ).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05112595 |
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| 출처 데이터셋 | uspto-grants-1992_05 |
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| ORD ID | ord-a608e555ca3c45e790ed0ca057610d93 |
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| 출처 메모 | uspto-grants-1992_05 |
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