تفاعل #805352

ord-70ee4656a8e340e5b40b9e13f7da8fd9

معادلة التفاعل

CCC[CH2][Sn]([Cl])([CH2]CCC)[CH2]CCC
tributyltin chloride
Cc1nccs1
2-methylthiazole
[Li][CH2]CCC
n-butyllithium
CCC[CH2][Sn]([CH2]CCC)([CH2]CCC)[c]1cnc(C)s1
2-methyl-5-(tributylstannyl)thiazole
المردود 85.2%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGstirred for an additional 1 h at −78° C
  2. 2
    workup.STIRRINGstirred for 1 h
  3. 3
    workup.ADDITIONtreated slowly with ice-cold satd
  4. 4
    استخلاصNaHCO3 (20 mL) and quickly extracted with Et2O (3×)
  5. 5
    غسيلThe combined organics were washed with brine
  6. 6
    تجفيفdried over Na2SO4
  7. 7
    تركيزconcentrated to dryness
  8. 8
    أخرىpurified via silica gel chromatography (EtOAc/Hex)

الإجراء التجريبي

A −78° C. solution of 2-methylthiazole (2 g, 20.17 mmol) in THF (50 mL) was treated drop-wise with n-butyllithium (2.5 M in Hex, 10.49 mL, 26.2 mmol), stirred for 1 h, treated drop-wise with a solution of tributyltin chloride (7.11 mL, 26.2 mmol) in THF (25 mL) and stirred for an additional 1 h at −78° C. The mixture was allowed to warm to RT, stirred for 1 h, treated slowly with ice-cold satd. NaHCO3 (20 mL) and quickly extracted with Et2O (3×). The combined organics were washed with brine, dried over Na2SO4, concentrated to dryness and purified via silica gel chromatography (EtOAc/Hex) to afford 2-methyl-5-(tributylstannyl)thiazole (6.67 g, 85%). 1H NMR (400 MHz, DMSO-d6): δ 7.55 (s, 1H), 2.67 (s, 3H), 1.54-1.45 (m, 6H), 1.30-1.23 (m, 6H), 1.09-1.04 (m, 6H), 0.83 (t, J=7.3 Hz, 9H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09193719B2uspto-grants-2015_11