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Lithium hydroxide, monohydrate → 3-[4-(2,3,4,5-Tetrahydro-benzo[b]azepine-1-carbonyl)-phenyl]-propionic Acid

HRID 220891
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HRID 220891 반응식
O.[OH-].[Li+].C[O:5][C:6](=[O:28])[CH2:7][CH2:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]([N:17]2[CH2:23][CH2:22][CH2:21][CH2:20][C:19]3[CH:24]=[CH:25][CH:26]=[CH:27][C:18]2=3)=[O:16])=[CH:11][CH:10]=1>O.O1CCOCC1>[N:17]1([C:15]([C:12]2[CH:11]=[CH:10][C:9]([CH2:8][CH2:7][C:6]([OH:28])=[O:5])=[CH:14][CH:13]=2)=[O:16])[CH2:23][CH2:22][CH2:21][CH2:20][C:19]2[CH:24]=[CH:25][CH:26]=[CH:27][C:18]1=2
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참가 물질

5

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 575553603-[4-(2,3,4,5-Tetrahydro-benzo[b]azepine-1-carbonyl)-phenyl]-propionic Acid Methyl Ester

생성물 1

HCID 575553343-[4-(2,3,4,5-Tetrahydro-benzo[b]azepine-1-carbonyl)-phenyl]-propionic Acid수율 61%

시약·촉매·용매 2

HCID 962Water용매HCID 312751,4-Dioxane용매

실험 절차

Lithium hydroxide monohydrate (114 mg, 2.72 mmol) was added to a solution of 3-[4-(2,3,4,5-tetrahydro-benzo[b]azepine-1-carbonyl)-phenyl]-propionic acid methyl ester from Example E65.3 (415 mg, 1.23 mmol) in water (5 ml) and dioxan (20 ml). The mixture was stirred for 18 h at room temperature then concentrated in vacuo. The residue was dissolved in chloroform, washed with 1M HCl solution then brine, dried and concentrated in vacuo to yield the title compound (241 mg, 61%).

후처리

  1. concentrationthen concentrated in vacuo
  2. dissolutionThe residue was dissolved in chloroform
  3. washwashed with 1M HCl solution
  4. dry with materialbrine, dried
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-8ce41a267ada44b6bf4c650b27d8eb6c
출처 데이터셋
uspto-grants-2012_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08202858B2

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