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Hydrochloric Acid → 4-(Benzyloxy)benzene-1,2-diamine

HRID 1679454
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반응식

HRID 1679454 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:4][C:3]=1[N+:16]([O-])=O.Cl.[OH-].[NH4+]>[Fe].CO>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:4][C:3]=1[NH2:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14923Ammonium HydroxideHCID 2614974-Benzyloxy-2-nitroaniline

생성물 1

HCID 131622394-(Benzyloxy)benzene-1,2-diamine

시약·촉매·용매 2

HCID 23925Iron촉매HCID 887Methanol용매

실험 절차

2.44 G. of 1-amino-4-benzyloxy-2-nitrobenzene is stirred in 100 ml. methanol and 100 ml. 20% hydrochloric acid with 1.0 g. iron powder at room temperature. After two hours, the mixture is poured into excess ammonium hydroxide solution, the residue extracted with chloroform, filtered under nitrogen, dried over magnesium sulfate, filtered once again, and evaporated to dryness to give 1,2-diamino-4-benzyloxybenzene.

후처리

  1. customat room temperature
  2. extractionthe residue extracted with chloroform
  3. filtrationfiltered under nitrogen
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered once again
  6. customevaporated to dryness

출처 및 근거

ORD 기록
ord-ba2497dcee00408e8a8915085b5eae18
출처 데이터셋
uspto-grants-1978_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04080461

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