Iodine → HCID 54064757, 화합물
반응식
[CH:1]([NH:3][C@H:4]([CH2:8][C:9]1[S:10][CH:11]=[CH:12][CH:13]=1)[C:5](O)=[O:6])=O.[BH4-].[Na+].II.CO>O1CCCC1>[CH3:1][NH:3][C@H:4]([CH2:8][C:9]1[S:10][CH:11]=[CH:12][CH:13]=1)[CH2:5][OH:6]참가 물질
반응 조건
- 온도
- 9.5 °C
실험 절차
A solution of (2R)-2-(formylamino)-3-(2-thienyl)propionic acid (3.58 g, 18.0 mmol) in tetrahydrofuran (50 ml) was added dropwise to a suspension of sodium borohydride in tetrahydrofuran (50 ml), which was cooled to 7-12° C. (inside temperature). After the addition was finished, a solution of iodine (4.57 g, 18.0 mmol) in tetrahydrofuran (100 ml) was added dropwise. The reaction mixture was heated to reflux for 16 h. It was cooled to 0° C. Methanol (200 ml) was added dropwise. The solvent was removed in vacuo. The residue was dissolved in a freshly prepared 20% aqueous sodium hydroxide solution (200 ml). The aqueous phase was extracted with tert-butyl methyl ether (4×150 ml). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo to give 3.26 g of crude (2R)-2-methylamino-3-(2-thienyl)propan-1-ol, which was used for the following step.
후처리
- additionAfter the addition
- temperatureThe reaction mixture was heated
- temperatureto reflux for 16 h
- temperatureIt was cooled to 0° C
- customThe solvent was removed in vacuo
- dissolutionThe residue was dissolved in a freshly prepared 20% aqueous sodium hydroxide solution (200 ml)
- extractionThe aqueous phase was extracted with tert-butyl methyl ether (4×150 ml)
- dry with materialThe combined organic layers were dried over magnesium sulfate
- customThe solvent was removed in vacuo
출처 및 근거
- ORD 기록
- ord-1c46c7ae2fd24b5b8682792bde4107f7
- 출처 데이터셋
- uspto-grants-1999_11
- 특허 번호
- US05977178
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