تفاعل #1833238

ord-1be1ce62e9ce4087b50c2722f4a51234

معادلة التفاعل

[Cl-].[NH4+]
NH4Cl
FC1(F)Oc2cc(Cl)c(Br)cc2O1
5-Bromo-6-chloro-2,2-difluorobenzo[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
CC1(C)OB(c2cc3c(cc2Cl)OC(F)(F)O3)OC1(C)C
title compound
المردود 101.8%
CC1(C)OB(c2cc3c(cc2Cl)OC(F)(F)O3)OC1(C)C
2-(6-Chloro-2,2-difluorobenzo[d][1,3]dioxol-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
المردود 101.8%

ظروف التفاعل

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

المعالجة

  1. 1
    workup.WAITwas continued for 45 min at 10-15° C
  2. 2
    غسيلThe organic phase was washed with saturated NaCl (10 mL)
  3. 3
    تجفيفdried (Na2SO4)
  4. 4
    أخرىevaporated

الإجراء التجريبي

5-Bromo-6-chloro-2,2-difluorobenzo[d][1,3]dioxole (1.0 g, 3.7 mmol) was dissolved in dry tetrahydrofuran (7 mL), cooled to 0-5° C. and treated in portions with isopropylmagnesium lithium chloride (1.3 M; 3.0 mL, 3.9 mmol). After 30 min, 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (730 mg, 4.0 mmol) was added, and stirring was continued for 45 min at 10-15° C. Saturated NH4Cl (10 mL) was added and the mixture was shaken with ethyl acetate (20 mL) and saturated NaCl (10 mL). The organic phase was washed with saturated NaCl (10 mL), dried (Na2SO4) and evaporated to give the title compound as a white solid (1.2 g, qt): 1H NMR (400 MHz, DMSO-d6) δ 7.64 (s, 1H), 7.53 (s, 1H), 1.30 (s, 12H); 19F NMR (376 MHz, DMSO-d6) δ −48.97 (s); EIMS m/z 318.

المصدر

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