تفاعل #1265388

ord-b5d2a21eba234f47b88bdf17c93bb46c

معادلة التفاعل

CC(=O)c1nccs1
1-Thiazol-2-yl-ethanone
COC(OC)OC
trimethyl orthoformate
Cc1ccc(S(=O)(=O)O)cc1
p-toluenesulfonic acid
COC(C)(OC)c1nccs1
sub-title compound
COC(C)(OC)c1nccs1
2-(1,1-Dimethoxy-ethyl)-thiazole

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
50°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe mixture was cooled to ambient and
  2. 2
    تركيزconcentrated
  3. 3
    أخرىpartitioned between saturated sodium bicarbonate and diethyl ether (100 ml)
  4. 4
    أخرىThe organic phase was removed
  5. 5
    غسيلwashed with saturated sodium bicarbonate and brine
  6. 6
    تجفيفdried (magnesium sulfate)
  7. 7
    ترشيحfiltered
  8. 8
    تركيزconcentrated

الإجراء التجريبي

To a solution of 1-Thiazol-2-yl-ethanone (7 g) in dry methanol (100 ml) was added trimethyl orthoformate (35 ml) and p-toluenesulfonic acid (10 g) and the resulting mixture was heated at 50° C. for 12 hours. The mixture was cooled to ambient and concentrated, partitioned between saturated sodium bicarbonate and diethyl ether (100 ml). The organic phase was removed and washed with saturated sodium bicarbonate and brine, dried (magnesium sulfate), filtered and concentrated to afford the sub-title compound as crude product. The product could be further purified if necessary by flash chromatography (20% ethyl acetate/petroleum ether) to afford the sub-title compound in quantitative yield as yellow oil (9.5 g); 1H NMR (400 Mhz, CDCl3) δ 1.75 (3H, s), 3.25 (6H, s), 7.3 (1H, s), 7.85 (1H, s); MS (ES+) 174.1 (M+1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07276502B2uspto-grants-2007_10