Acetic Acid → 5-Acetylamino-2,3-dihydrobenzofuran

反応式

Cl.O1C2C=C[C:9]([C:11](=[N:13]O)[CH3:12])=[CH:10]C=2CC1.[CH3:15][C:16]([O:18][C:19]([CH3:21])=O)=O.[CH3:22][C:23](O)=[O:24]>>[O:18]1[C:19]2[CH:21]=[CH:12][C:11]([NH:13][C:23](=[O:24])[CH3:22])=[CH:9][C:10]=2[CH2:15][CH2:16]1

参加物

反応物 4

HCID 176Acetic Acid

HCID 313Hydrochloric Acid

HCID 7918Acetic Anhydride

HCID 28214741-(2,3-Dihydro-1-benzofuran-5-yl)ethanone oxime

生成物 1

HCID 129085765-Acetylamino-2,3-dihydrobenzofuran収率 52%

実験手順

NH2OH.HCl (7.3 g, 105 mmol) was added to a stirred solution of ketone 191 (14.2 g, 87.7 mmol) and pyridine (9.2 mL, 114 mmol) in MeOH (100 mL) and the mixture stirred at 20° C. for 16 h. The solvent was evaporated and the residue partitioned between brine and EtOAc. The organic fraction was dried and the solvent evaporated to give crude 1-(2,3-dihydro-1-benzofuran-5-yl)ethanone oxime (15.3 g, 99%). HCl gas was bubbled through a solution of the oxime (15.3 g, 86.5 mmol) in Ac2O (16.3 mL, 173 mmol) and HOAc (54 mL, 865 mmol), and the solution stood at 20° C. for 24 h. The precipitate was poured into ice/water, stirred for 2 h, the solid filtered and washed with water and dried. The aqueous fraction was extracted with DCM (2×50 mL), the combined organic extract dried and the solvent evaporated. The slurry was treated with water (20 mL) and evaporated several times to remove Ac2O. The combined solids were purified by chromatography, eluting with a gradient (50-100%) of EtOAc/pet. ether, to give acetamide 192 (7.94 g, 52%) as a white solid: mp 92-93° C. [lit. (Blade-Font, A.; de Mas Rocabayera, T. J. Chem. Soc. P1, 1982, 814848) mp 93° C.]; 1H NMR δ 7.47 (br s, 1H, H-4), 7.21 (br s, 1H, NH), 6.99 (dd, J=8.5, 2.1 Hz, 1H, H-6), 6.69 (d, J=8.5 Hz, 1H, H-7), 4.55 (t, J=8.7 Hz, 2H, H-2), 3.18 (br t, J=8.7 Hz, 2H, H-3), 2.13 (s, 3H, CH3).