Hydrochloric Acid → 4-Hydroxy-4'-octylazobenzene

HRID 867354

반응식

HRID 867354 반응식
[CH2:1]([C:9]1[CH:15]=[CH:14][C:12]([NH2:13])=[CH:11][CH:10]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].Cl.[N:17]([O-])=O.[Na+].[OH-].[Na+].[C:23]1([OH:29])[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>O>[OH:29][C:23]1[CH:28]=[CH:27][C:26]([N:17]=[N:13][C:12]2[CH:11]=[CH:10][C:9]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])=[CH:15][CH:14]=2)=[CH:25][CH:24]=1

참가 물질

7

실험 절차

35 g (0.17M) of 4-octylaniline was cooled to 0° C. or below, 85 g of10% aqueous hydrochloric acid solution was added, and then a solution of 12.0 g of sodium nitrite in 68 ml of water was added. During the addition,the mixture was cooled so as not to exceed 0° C. After the addition,the mixture was allowed to react for 30 minutes, transferred into a dropping funnel and added dropwise into 170 g of an 8% NaOH aqueous solution containing 16 g of phenol held at 5° C. or below. After the addition, the mixture was stirred for 1 hour, and then 10% hydrochloric acid aqueous solution was added thereto until a pH of 5-6 toprecipitate the reaction product. The precipitate was separated by filtration, washed with water and dried overnight under reduced pressure. After the drying, the product was washed with 500 ml of petroleum ether and further dried under reduced pressure to obtain 30.8 g (0.10M) of 4-hydroxy-4'-octylazobenzene. The yield was 59%.

후처리

  1. temperatureDuring the addition,the mixture was cooled so as not
  2. customto exceed 0° C
  3. customto react for 30 minutes
  4. customtransferred into a dropping funnel
  5. customheld at 5° C. or below
  6. additionAfter the addition
  7. customThe precipitate was separated by filtration
  8. washwashed with water
  9. customdried overnight under reduced pressure
  10. washAfter the drying, the product was washed with 500 ml of petroleum ether
  11. customfurther dried under reduced pressure

출처 및 근거

ORD 기록
ord-e519b6dfa6e94381bd4fad218d7d3c12
출처 데이터셋
uspto-grants-1988_10
특허 번호
US04775223

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