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Methyl 2-(2-benzyloxyphenyl)-5-nitrobenzoate → 8-Aminobenzo[c]chromen-6-one

HRID 909286
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반응식

HRID 909286 반응식
C(O[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]1[CH:24]=[CH:23][C:22]([N+:25]([O-])=O)=[CH:21][C:16]=1[C:17]([O:19]C)=[O:18])C1C=CC=CC=1>CO.O1CCCC1.[Pd]>[NH2:25][C:22]1[CH:23]=[CH:24][C:15]2[C:10]3[C:9](=[CH:14][CH:13]=[CH:12][CH:11]=3)[O:19][C:17](=[O:18])[C:16]=2[CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 58026868Methyl 2-(2-benzyloxyphenyl)-5-nitrobenzoate

생성물 1

HCID 233789368-Aminobenzo[c]chromen-6-one수율 73%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 8028Tetrahydrofuran용매

실험 절차

Methyl 2-(2-benzyloxyphenyl)-5-nitrobenzoate (Reference Compound No. 1-1-(1), 21.0 g, 57.8 mmol) was dissolved in a mixture of methanol (135 mL) and tetrahydrofuran (90 mL), then 5% palladium on charcoal (2.19 g) was added thereto, and then the reaction mixture was stirred under hydrogen atmosphere at room temperature overnight. After the unsoluble materials were filtered, the filtrate was removed under reduced pressure. A mixture of ethyl acetate and hexane was added to the obtained residue, and then the mixture was filtered to give the titled reference compound (8.92 g) as a pale yellow solid. (Yield 73%)

후처리

  1. filtrationAfter the unsoluble materials were filtered
  2. customthe filtrate was removed under reduced pressure
  3. additionA mixture of ethyl acetate and hexane
  4. additionwas added to the obtained residue
  5. filtrationthe mixture was filtered

출처 및 근거

ORD 기록
ord-abceab85593e42bc949466890ab36a64
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08017775B2

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