참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl iodide | HCID 6328 | — |
| 반응물 | Diisopropylamine | HCID 7912 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | (R)-Benzyl (5-oxotetrahydrofuran-3-yl)carbamate | HCID 697924 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 촉매 | ICE protocol 1 | HCID 56841950 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | Benzyl ((3R,4R)-4-methyl-5-oxotetrahydrofuran-3-yl)carbamate | HCID 13108321 | — |
반응 단계
272 μl (1.9 mmol) diisopropylamine are placed in 3 ml THF and while cooling with ice 1.2 ml (1.9 mmol) of an n-butyllithium solution in hexane (1.6M) are added. The mixture is stirred for 10 minutes at 0° C., then cooled to −78° C. and a solution of 200 mg (0.85 mmol) benzyl (R)-(5-oxo-tetrahydrofuran-3-yl)-carbamate in 1 ml THF is added dropwise. The mixture is stirred for one hour at −78° C. Then 210 μl (3.3 mmol) methyl iodide are added dropwise, and the mixture is heated to −60° C. within one hour. Then 0.5 ml sat. ammonium chloride solution is added and the mixture is heated to ambient temperature. Water is added and the mixture is extracted three times with ethyl acetate. The combined organic phases are dried over sodium sulphate and evaporated to dryness. The residue is taken up in DMF, acidified with TFA and purified by reversed-phase chromatography.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07615549B2 |
|---|
| 출처 데이터셋 | uspto-grants-2009_11 |
|---|
| ORD ID | ord-5b312c38ffbe4103ae25f7061656ab9e |
|---|
| 출처 메모 | uspto-grants-2009_11 |
|---|