Pyridine → N-[3-(Hydroxymethyl)phenyl]-4-(tetradecyloxy)benzamide

HRID 483560

반응식

HRID 483560 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH2:5][OH:6].N1C=CC=CC=1.[CH2:16]([O:30][C:31]1[CH:39]=[CH:38][C:34]([C:35](Cl)=[O:36])=[CH:33][CH:32]=1)[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29].C(Cl)(Cl)Cl>C(Cl)Cl.O>[OH:6][CH2:5][C:4]1[CH:3]=[C:2]([NH:1][C:35](=[O:36])[C:34]2[CH:33]=[CH:32][C:31]([O:30][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])=[CH:39][CH:38]=2)[CH:9]=[CH:8][CH:7]=1

참가 물질

7

실험 절차

To a solution of 8.17 g of m-aminobenzyl alcohol and 16.14 g of pyridine in 200 ml of methylene chloride is added at 0° C. over 30 minutes a solution of 18 g of p-tetradecyloxybenzoyl chloride in 200 ml of methylene chloride. Stirring is continued for another 6 hours. An additional 400 ml of chloroform and water is added followed by warming to dissolve all the solids. The warm organic layer is separated and washed with dilute hydrochloric acid and saturated sodium bicarbonate. The warm organic layer is dried and filtered. The filtrate is diluted with an equal volume of hexane and cooled in a refrigerator overnight. The resulting solid is collected and air dried to give 18.4 g of the desired product as a white solid, m.p. 112°-115° C.

후처리

  1. temperatureby warming
  2. dissolutionto dissolve all the solids
  3. customThe warm organic layer is separated
  4. washwashed with dilute hydrochloric acid and saturated sodium bicarbonate
  5. customThe warm organic layer is dried
  6. filtrationfiltered
  7. additionThe filtrate is diluted with an equal volume of hexane
  8. temperaturecooled in a refrigerator overnight
  9. customThe resulting solid is collected
  10. customair dried

출처 및 근거

ORD 기록
ord-ee6686cdafc5499fad2c7154160a53da
출처 데이터셋
uspto-grants-1993_07
특허 번호
US05225425

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