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Hydrochloric Acid → HCID 19838093, 화합물

HRID 1381607
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HRID 1381607 반응식
C([O:4][C:5]1[C:6]([CH2:18][CH2:19][CH3:20])=[C:7]([CH:10]=[C:11]([N+:15]([O-:17])=[O:16])[C:12]=1[O:13][CH3:14])[CH:8]=[O:9])(=O)C.Cl>[OH-].[Na+]>[OH:4][C:5]1[C:6]([CH2:18][CH2:19][CH3:20])=[C:7]([CH:10]=[C:11]([N+:15]([O-:17])=[O:16])[C:12]=1[O:13][CH3:14])[CH:8]=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 212762813-Acetyloxy-4-methoxy-5-nitro-2-propylbenzaldehyde

생성물 1

HCID 19838093HCID 19838093, 화합물수율 98.2%

시약·촉매·용매 1

HCID 14798Sodium Hydroxide용매

실험 절차

A suspension of the product from step (b) (39.5 g) in 20% sodium hydroxide solution (140 ml) was heated at 90° for 5 hours. The mixture was cooled and acidified wth dilute hydrochloric acid. The aqueous phase was extracted with ethyl acetate washed with brine, dried, filtered and evaporated to leave a brown oil (33 g) MS; m/e 239.

후처리

  1. temperaturewas heated at 90° for 5 hours
  2. temperatureThe mixture was cooled
  3. extractionThe aqueous phase was extracted with ethyl acetate
  4. washwashed with brine
  5. customdried
  6. filtrationfiltered
  7. customevaporated

출처 및 근거

ORD 기록
ord-4104587e60c046ad935a7b6e73e786f9
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04803225

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