تفاعل #1833222

ord-56cc370753734e4696f4b9d023c42712

معادلة التفاعل

Fc1c(Br)ccc2c1OC(F)(F)O2
5-Bromo-2,2,4-trifluorobenzo[d][1,3]dioxole
C[CH](C)[Mg][Cl].[Cl-].[Li+]
isopropylmagnesium chloride lithium chloride
CC(C)OB1OC(C)(C)C(C)(C)O1
2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CC1(C)OB(c2ccc3c(c2F)OC(F)(F)O3)OC1(C)C
title compound
المردود 72.4%
CC1(C)OB(c2ccc3c(c2F)OC(F)(F)O3)OC1(C)C
4,4,5,5-Tetramethyl-2-(2,2,4-trifluorobenzo[d][1,3]dioxol-5-yl)-1,3,2-dioxaborolane
المردود 72.4%

ظروف التفاعل

درجة الحرارة
-20°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirring
  2. 2
    workup.WAITwas continued for 1 h at 10-15° C
  3. 3
    غسيلThe organic phase was washed with saturated NaCl (15 mL)
  4. 4
    تجفيفdried (Na2SO4)
  5. 5
    أخرىevaporated

الإجراء التجريبي

5-Bromo-2,2,4-trifluorobenzo[d][1,3]dioxole (4.0 g, 16 mmol) was dissolved in 20 mL dry tetrahydrofuran, cooled to −20° C. and treated with isopropylmagnesium chloride-lithium chloride complex (1.3 M in tetrahydrofuran; 13 mL, 17 mmol) in portions over 10 min. After stirring for 30 min at −20 to 0° C., 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (3.1 g, 17 mmol) was added, and stirring was continued for 1 h at 10-15° C. After treatment with saturated NH4Cl solution (10 mL), the mixture was diluted with ethyl acetate (50 mL). The organic phase was washed with saturated NaCl (15 mL), dried (Na2SO4) and evaporated to give the title compound as a brown solid (3.5 g, 72%): 1H NMR (400 MHz, CDCl3) δ 7.46 (d, J=26.5 Hz, 1H), 6.90 (dd, J=18.5, 4.5 Hz, 1H), 1.35 (s, 12H); 19F NMR (376 MHz, CDCl3) δ −49.70 (s), −126.00 (s); EIMS m/z 302.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09149038B2uspto-grants-2015_10