تفاعل #51206

ord-967ddfe73b30491d9915c6116112b85f

معادلة التفاعل

Cl
HCl
C=O
paraformaldehyde
Cc1cccc(O)c1
3-methyl-phenol
[Cl][Sn]([Cl])([Cl])[Cl]
SnCl4
Cc1ccc(C=O)c(O)c1
title product
المردود 25.5%
Cc1ccc(C=O)c(O)c1
2-Hydroxy-4-methyl-benzaldehyde
المردود 25.5%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    استخلاصThe solution was extracted with ether (25 ml)
  2. 2
    غسيلwashed with brine (20 ml)
  3. 3
    تجفيفdried (MgSO4)
  4. 4
    ترشيحfiltered
  5. 5
    أخرىevaporated to a brown oil
  6. 6
    أخرىThis oil was purified by column chromatography

الإجراء التجريبي

To a stirred solution of 3-methyl-phenol (1 g, 9.2 mmol) in toluene (5 ml) at room temperature under nitrogen was added SnCl4 (241 mg, 0.92 mmol) and tri-nbutylamine (0.6 ml, 2.77 mmol). After 20 min, paraformaldehyde (611 mg, 20.3 mmol) was added and the whole stirred at 100° C. for 16 h. The reaction mixture was diluted with water (20 ml) and acidified with 2N HCl to pH2. The solution was extracted with ether (25 ml), washed with brine (20 ml), dried (MgSO4) filtered and evaporated to a brown oil. This oil was purified by column chromatography using 5% EtOAc in pentane as eluant to provide the title product (319 mg, 25%); 1HNMR (400 MHz, CDCl3) δ: 2.3 (s, 3H), 6.75 (m, 2H), 7.35 (d, 1H), 9.75 (s, 1H), 11.00 (s, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849649B2uspto-grants-2005_02