Water → 4-Methyl-3-thiopheneboronic acid
반응식
CC1(C)C(C)(C)[O:5][B:4]([C:9]2[C:13]([CH3:14])=[CH:12][S:11][CH:10]=2)[O:3]1.O>CC(C)=O>[CH3:14][C:13]1[C:9]([B:4]([OH:5])[OH:3])=[CH:10][S:11][CH:12]=1참가 물질
4
실험 절차
A solution of 4,4,5,5-tetramethyl-2-(4-methyl-thiophen-3-yl)-[1,3,2]dioxaborolane (3.69 g, 16.47 mmol) in acetone (30 mL) is treated with H2O (30 mL), followed by NaIO4 (7.05 g, 32.95 mmol). The resulting mixture is stirred at rt overnight. The organic solvent is removed in vacuo. The residue is diluted with H2O (50 mL), extracted with EtOAc ((2×100 mL). The organic extracts are combined, dried with Na2SO4, filtered and concentrated. Purification of the crude material by chromatography gives the title compound (0.82 g, 5.78 mmol, 35%). 1H NMR (CDCl3): δ 1.33 (s, 3H), 2.64-2.66 (m, 2H), 7.00-7.02 (m, 1H), 8.27 (d, J=3.0 Hz, 1H). ES-MS (m/z): calcd for C5H7BO2S (M−H)−: 141.0; found: 141.1.
후처리
- customThe organic solvent is removed in vacuo
- additionThe residue is diluted with H2O (50 mL)
- extractionextracted with EtOAc ((2×100 mL)
- dry with materialdried with Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customPurification of the crude material by chromatography
출처 및 근거
- ORD 기록
- ord-a8a30ceb476343bbae7eb70893bc2549
- 출처 데이터셋
- uspto-grants-2009_11
- 특허 번호
- US07612067B2
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