تفاعل #5446

ord-0c78cd059b394bef950f6b265b6865dc

معادلة التفاعل

CCN(C(C)C)C(C)C
diisopropyl ethyl amine
CCOC(OCC)OCC
Triethyl orthoformate
COc1ccc(Br)c2c1C(=O)CC2
product
COc1ccc(Br)c2c1C(=O)CC2
4-Bromo-7-methoxy-2,3-dihydro-1H-inden-1-one
CCOCC.FB(F)F
BF3.Et2O
CCOC(OCC)C1Cc2c(Br)ccc(OC)c2C1=O
white solid
CCOC(OCC)C1Cc2c(Br)ccc(OC)c2C1=O
4-Bromo-7-methoxy-1-oxo-2,3-dihydro-1H-indene-2-carboxaldehyde diethy acetal

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةcooled to -78° C
  2. 2
    درجة الحرارةThe reaction was then warmed to -15° C. for 2 h
  3. 3
    أخرىquenched in 5% NaHCO3 solution
  4. 4
    استخلاصextracted with methylene chloride
  5. 5
    غسيلThe organic extracts were washed with brine
  6. 6
    تجفيفdried (MgSO4)
  7. 7
    أخرىthe solvent removed
  8. 8
    أخرىThe crude product was triturated with cold hexane
  9. 9
    أخرىthe crystalline product collected

الإجراء التجريبي

Triethyl orthoformate (16.5 ml) was cooled to -30° C. and 15.0 ml BF3.Et2O in 50 ml methylene chloride was added. The reaction was warmed to 0° C. for 15 min, and then cooled to -78° C. To the reaction was added 12.05 g of the product from Example 34 in 50 ml methylene chloride, followed by dropwise addition of 19.4 ml diisopropyl ethyl amine. The reaction was then warmed to -15° C. for 2 h, then quenched in 5% NaHCO3 solution and extracted with methylene chloride. The organic extracts were washed with brine, dried (MgSO4), and the solvent removed. The crude product was triturated with cold hexane, and the crystalline product collected to yield 14.60 g of a white solid, mp: 76°-8° C. NMR (CDCl3) δ 1.05 (t, 3H), 1.27 (t, 3H), 3.03 (m, 2 H), 3.30 (m, 1H), 3.43-3.80 (m, 4H), 3.95 (s, 3H), 5.00 (d, 1H), 6.71 (d, 1H), 7.63 (d, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05244888uspto-grants-1993_09