تفاعل #57568

ord-3f44d056d2ef4778a58629bd5e844bbb

معادلة التفاعل

C#Cc1cccc2oc(C(=O)OCC)c(C)c12
4-ethynyl-3-methyl-benzofuran-2-carboxylic acid ethyl ester
CC(C)(C)OC(=O)OC(=O)OC(C)(C)C
di-tert-butyl dicarbonate
CC[N+](=O)[O-]
Nitroethane
CCOC(=O)c1oc2cccc(-c3cc(C)no3)c2c1C
3-methyl-4-(3-methyl-isoxazol-5-yl)-benzofuran-2-carboxylic acid ethyl ester
المردود 25.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

To a solution of 4-ethynyl-3-methyl-benzofuran-2-carboxylic acid ethyl ester (228 mg, 0.99 mmol, 1 eq.) in acetonitrile (5 mL) under argon, was added di-tert-butyl dicarbonate (327 mg, 1.5 mmol, 1.5 eq.), and 4-(dimethylamino)pyridine (12 mg, 0.1 mmol, 0.1 eq.). Nitroethane (79 uL, 1.1 mmol, and 1.1 eq.) in acetonitrile (5 mL) was added drop-wise to the reaction mixture, and the reaction was stirred at room temperature for 72 hours. After work-up and flash column chromatography, 3-methyl-4-(3-methyl-isoxazol-5-yl)-benzofuran-2-carboxylic acid ethyl ester was obtained in 25% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.4 (t, J=7.1 Hz, 3 H) 2.3 (s, 3 H) 2.4 (s, 3 H) 4.4 (q, J=7.1 Hz, 2 H) 6.8 (s, 1 H) 7.5 (dd, J=7.5, 0.9 Hz, 1 H) 7.6 (m, 1 H) 7.9 (dd, J=8.5, 0.9 Hz, 1 H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07420001B2uspto-grants-2008_09