반응 #1256708

ord-78d5ab97210147188cf12bb693d0adce

반응 방정식

Cl
hydrochloric acid
N#N
N2
[Na+].[OH-]
NaOH
COc1cc(C)c(-c2c(C)cncc2C)c(C)c1
4
COc1cc(C)c(-c2c(C)cncc2C)c(C)c1
4-(4-methoxy-2,6-dimethyl-phenyl)-3,5-dimethyl-pyridine
Cc1cncc(C)c1-c1c(C)cc(O)cc1C
4-(3,5-dimethyl-pyridin-4-yl)-3,5-dimethyl-phenol

반응 조건

온도
140°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.DISTILLATIONwas distilled from the mixture until the temperature
  2. 2
    기타rose to 210° C
  3. 3
    기타the reaction flask was fitted with a reflux condenser
  4. 4
    온도refluxed for 3 h at 210° C
  5. 5
    기타The resulting reaction mixture
  6. 6
    여과The resulting colorless precipitate was then collected by filtration
  7. 7
    세척washed with water
  8. 8
    기타to give 0.208 g (91.6%) of analytically pure product as a colorless solid

실험 절차

To stirring pyridine (3 mL) was slowly added concentrated hydrochloric acid (3.3 mL). The reaction flask was then fitted for distillation, and water was distilled from the mixture until the temperature rose to 210° C. After cooling to 140° C., 4 (0.241 g, 1.00 mmol) was added to the above mixture, and the reaction flask was fitted with a reflux condenser connected to a N2 source. The yellow mixture was stirred and refluxed for 3 h at 210° C. The resulting reaction mixture was then diluted with warm water (3 mL) and slowly poured into hot water (20 mL). The resulting yellow solution was cooled to room temperature and neutralized with dilute NaOH solution to pH ˜7. The resulting colorless precipitate was then collected by filtration and washed with water to give 0.208 g (91.6%) of analytically pure product as a colorless solid: mp>270° C. (decomp.); 1H NMR (500 MHz, DMSO-d6): δ 9.245 (s, 1H), 8.337 (s, 2H), 6.579 (s, 2H), 1.841 (s, 6H), 1.729 (s, 6H); 13C NMR (125 MHz, DMSO-d6): δ 156.400, 148.191, 147.630, 134.949, 131.015, 127.197, 114.493, 19.359, 16.098; MS (ESI): m/z 228.4 [(M+H)+, 100]; Anal. Calcd. For C15H17NO: C, 79.26; H, 7.54; N, 6.16. Found: C, 79.14; H, 7.58; N, 6.18.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07824582B2uspto-grants-2010_11