Benzaldehyde → 4-Benzyl-1,7-diphenyl-1,6-heptadiene-3,5-dione

HRID 714154

반응식

HRID 714154 반응식
[CH2:1]([CH:8]([C:12](=[O:14])[CH3:13])[C:9](=[O:11])[CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:15](=O)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.B(OCCCC)(OCCCC)O[CH2:25][CH2:26][CH2:27]C.[CH2:39](N)[CH2:40][CH2:41][CH3:42].Cl>C(OCC)(=O)C>[CH2:1]([CH:8]([C:9](=[O:11])[CH:10]=[CH:42][C:41]1[CH:27]=[CH:26][CH:25]=[CH:39][CH:40]=1)[C:12](=[O:14])[CH:13]=[CH:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

7

실험 절차

Boric anhydride (0.49 g, 7.0 mmol) was combined with 3-benzyl-2,4-pentanedione (8, 1.90 g, 10.0 mmol) and stirred for 48 hr at room temperature under a nitrogen atmosphere. A solution of dry ethyl acetate (10 ml), benzaldehyde (1b, 2.05 ml, 20.2 mmol) and tributyl borate (11.0 ml, 40.5 mmol) was added and the mixture stirred for 15 min at room temperature. Butylamine (0.20 ml, 2.0 mmol) was added dropwise over 30 min and stirring was continued for 18 hr at room temperature. Hydrochloric acid (15 ml, 0.4 N) was warmed to 60° C., added to the mixture and stirring was continued for 1 hr. The resulting mixture was filtered to afford a solid. The crude solid was triturated with methanol to give 2.30 g (63%) of a yellow solid: mp 162-164° C. [expected mp 156-158° C.]; 1H NMR: δ 3.99 (s, 2H), 6.99 (d, 2H, J=15.6 Hz), 7.34 (m, 15H), 7.77 (d, 2H, J=15.2 Hz); 13C NMR: δ 31.8, 109.3, 120.8, 126.5, 127.8, 128.1, 128.8, 130.0, 135.3, 140.5, 141.9, 183.6.

후처리

  1. stirringthe mixture stirred for 15 min at room temperature
  2. stirringstirring
  3. waitwas continued for 18 hr at room temperature
  4. additionadded to the mixture
  5. stirringstirring
  6. waitwas continued for 1 hr
  7. filtrationThe resulting mixture was filtered
  8. customto afford a solid
  9. customThe crude solid was triturated with methanol

출처 및 근거

ORD 기록
ord-5c9d7cb901ef403d94e6dc554e231ee0
출처 데이터셋
uspto-grants-2015_11
특허 번호
US09187397B2

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