참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 3,4-Dichlorobenzaldehyde | HCID 22710 | — |
| 반응물 | Trimethylsilyl cyanide | HCID 82115 | — |
| 반응물 | Borane;tetrahydrofuran | HCID 2723981 | — |
| 촉매 | zinc(II)iodide | HCID 9883512 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | alpha-(Aminomethyl)-3,4-dichlorobenzenemethanol | HCID 19349 | 772% |
반응 단계
To a mixture of 3,4-dichlorobenzaldehyde (3.50 g, 20.2 mmol) and ZnI2 (19 mg, 0.06 mmol) at 0° C. was added TMSCN (2.2 g, 2.2 mmol). The reaction mixture was stirred at 0° C. for 10 min and then warmed to rt and stirred for an additional 1 h. The mixture was concentrated to afford an orange-brown colored oil. The oil was dissolved in THF (20 mL) and BH3.THF (1 M in THF; 25 mL, 25 mmol) was added at 0° C. The reaction mixture was warmed to rt and stirred overnight. The mixture was cooled to 0° C. and MeOH (6 mL) was added with continued stirring for 2 h. After being warmed to rt, the mixture was concentrated. The residue was dissolved in MeOH (10 mL) and HCl (2 M in Et2O; 25 mL) was added at 0° C. After 30 min, Et2O (100 mL) was added and the resulting white solid was filtered and washed with Et2O (2×50 mL) to give a white solid (3.5 g, 72%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08598202B2 |
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| 출처 데이터셋 | uspto-grants-2013_12 |
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| ORD ID | ord-0689aa7f7264494d988f565bb322fb78 |
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| 출처 메모 | uspto-grants-2013_12 |
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