تفاعل #1833237

ord-874d5c44b6ca438b95ba84a71dbf649b

معادلة التفاعل

[Cl-].[NH4+]
NH4Cl
COc1cc2c(cc1I)OC(F)(F)O2
2,2-Difluoro-5-iodo-6-methoxybenzo[d][1,3]dioxole
C[CH](C)[Mg+].[Cl-].[Cl-].[Li+]
isopropylmagnesium lithium chloride
[Cl-].[Na+]
NaCl
CC(C)OB1OC(C)(C)C(C)(C)O1
2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
COc1cc2c(cc1B1OC(C)(C)C(C)(C)O1)OC(F)(F)O2
title compound
COc1cc2c(cc1B1OC(C)(C)C(C)(C)O1)OC(F)(F)O2
2-(2,2-Difluoro-6-methoxybenzo[d][1,3]dioxol-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

ظروف التفاعل

درجة الحرارة
2.5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITwas continued for 40 min at 15-20° C
  2. 2
    غسيلThe organic phase was washed with saturated NaCl (10 mL)
  3. 3
    تجفيفdried (Na2SO4)
  4. 4
    أخرىevaporated

الإجراء التجريبي

2,2-Difluoro-5-iodo-6-methoxybenzo[d][1,3]dioxole (1.6 g, 5.0 mmol) was dissolved in dry tetrahydrofuran (15 mL), cooled to 0-5° C. and treated in portions with isopropylmagnesium lithium chloride (1.3 M; 4.1 mL, 5.3 mmol). After 50 min, 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.0 g, 5.4 mmol) was added and stirring was continued for 40 min at 15-20° C. The mixture was treated with saturated NH4Cl (10 mL) and then mixed with saturated NaCl (10 mL) and ethyl acetate (20 mL). The organic phase was washed with saturated NaCl (10 mL), dried (Na2SO4) and evaporated to give title compound as a thick oil which was used without further purification (1.4 g, 89%): 1H NMR (400 MHz, CDCl3) δ 7.35 (s, 1H), 6.65 (s, 1H), 3.81 (s, 3H), 1.34 (s, 12H); 19F NMR (376 MHz, CDCl3) δ −50.17 (s); EIMS m/z 314.

المصدر

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