Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonia → {[(2R)-oxolan-2-yl]methyl}thiourea
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Hydrogen Peroxide | HCID 784 | — |
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | (R)-(-)-Tetrahydrofurfurylamine | HCID 2734124 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | {[(2R)-oxolan-2-yl]methyl}thiourea | HCID 1810731 | — |
반응 단계
To a 0° C. solution of (R)-(tetrahydrofuran-2-yl)methanamine (5.0 g, 49.5 mmol) and triethylamine (690 uL, 4.95 mmol) in tetrahydrofuran (100 mL) was added carbon disulfide (5.65 g, 74.3 mmol). Stirring was continued for 0.5 hour followed by the dropwise addition of 30% hydrogen peroxide (5.6 g, 49.5 mmol) so that the temperature was maintained below 40° C. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic extract was dried (Na2SO4), filtered and concentrated to afford an oil. The residue was dissolved in tetrahydrofuran, and treated with 7 N ammonia in methanol (14.3 mL, 100 mmol). The precipitate was collected by filtration and washed with water to afford the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08841334B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-ab61ef12de984805b7afab8d21846160 |
| 출처 메모 | uspto-grants-2014_09 |