반응 #1946561

ord-75850a36f1a24abb9732c11e16c87418

반응 방정식

CCCCN(CCCC)c1nc(-c2cccc(OC)c2)cs1
2-di-n-butylamino-4-(3-methoxyphenyl)thiazole
CCCCN(CCCC)c1nc(-c2cccc(OC)c2)cs1
compound 2-12
CCCCN(CCCC)c1nc(-c2cccc(OC)c2)cs1
2-di-n-butylamino-4-(3-methoxyphenyl)thiazole
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
O=P(Cl)(Cl)Cl
phosphorus oxychloride
CCCCN(CCCC)c1nc(-c2cccc(OC)c2)c(C=O)s1
2-Dibutylamino-4-(3-methoxyphenyl)-5-thiazolecarboxaldehyde

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    추출The oily precipitate was extracted with methylene chloride
  2. 2
    세척the extract was washed with water
  3. 3
    건조dried over magnesium sulfate
  4. 4
    농축concentrated
  5. 5
    기타was used without further purification

실험 절차

To a solution of 100.8 g (316.5 mmol) of crude 2-di-n-butylamino-4-(3-methoxyphenyl)thiazole (compound 2-12) and 630 ml of DMF was added, over about 30 mins, a solution of 55.81 g (364 mmol) of phosphorus oxychloride in 188 ml of DMF. The mixture was stirred overnight and poured into a solution of 158.1 g of sodium carbonate in 3.5 l of water. The oily precipitate was extracted with methylene chloride, and the extract was washed with water, dried over magnesium sulfate, and concentrated. The yield of brown oil was 88.77 g and was used without further purification. Anal. Calcd. For C19H26N2O2S: C, 65.9; H, 7.6; N, 8.1; S, 9.3. Found: C, 66.20; H, 7.85; N, 8.60; S, 7.93.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US06528223B1uspto-grants-2003_03