Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → N-Benzyl-N-(trimethylsilylmethyl)aminoacetonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Potassium Cyanide | HCID 9032 | — |
| 반응물 | N-[(Trimethylsilyl)methyl]benzylamine | HCID 353458 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-Benzyl-N-(trimethylsilylmethyl)aminoacetonitrile | HCID 560960 | 100.5% |
반응 단계
1 N Hydrochloric acid solution (119 mL) was added to N-benzyl-N-trimethylsilanylmethyl-amine (23.00 g, 119 mmol) and white precipitate formed. Tetrahydrofuran (650 mL), potassium cyanide (9.3 g, 143 mmol), and aqueous formaldehyde solution (37 wt. %, 12 mL, 155 mmol) were added to the reaction mixture and stirred at ambient temperature for 15 hours. The mixture was extracted with ether and separated and the combined organic layers were washed with water, dried over magnesium sulfate, and concentrated sequentially under reduced pressure and high vacuum at ambient temperature to afford 27.80 g of (N-Benzyl-N-trimethylsilanylmethyl-amino)acetonitrile.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07879849B2 |
| 출처 데이터셋 | uspto-grants-2011_02 |
| ORD ID | ord-c4b398f741d14dda90ff25337c8387d0 |
| 출처 메모 | uspto-grants-2011_02 |