تفاعل #1253204

ord-a6d5cc91630245bc8804d18c7cc538b6

معادلة التفاعل

CCCCCCCc1ccccc1
Phenylheptane
BrBr
bromine
CCCCCCCc1ccc(Br)cc1
pure product
CCCCCCCc1ccc(Br)cc1
1-Bromo-4-heptylbenzene

الكواشف

لا شيء

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    أخرىthe reaction was quenched with 1N KOH
  2. 2
    استخلاصAfter extraction
  3. 3
    غسيلthe organic phase was washed with water
  4. 4
    تجفيفdried over MgSO4
  5. 5
    أخرىwas purified by column chromatography on silica gel

الإجراء التجريبي

Phenylheptane (100 g, 0.57 mol) was dissolved in 900 mL of chloroform, and ferric chloride (1.41 g, 9 mmol) was added. The mixture was cooled to 0° C. and bromine (32 mL, 0.62 mmol) was added dropwise through an additional funnel. The reaction was kept in dark to prevent the bromination of the aliphatic side chain. After stirring at room temperature overnight, the reaction was quenched with 1N KOH. After extraction, the organic phase was washed with water and dried over MgSO4. The crude product was a brown oil and was purified by column chromatography on silica gel using heptane as an eluent to give 60 g of pure product as light yellow oil at 42% yield. 1H NMR (CDCl3) δ (ppm): 0.88 (t, J=6.9 Hz, 3H), 1.26-1.31 (m, 8H), 1.54-1.59 (m, 2H), 2.54 (t, J=7.8 Hz, 2H), 7.04 (d, J=8.2 Hz, 2H), 7.38 (d, J=8.2 Hz, 2H). FD-MS: m/z 255 (M+).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06613457B2uspto-grants-2003_09