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Hydrochloric Acid → (2-{3-[2-(1-Adamantyl)ethoxy]phenyl}ethyl)amine

HRID 1925501
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반응식

HRID 1925501 반응식
[C:1]12([CH2:11][CH2:12][O:13][C:14]3[CH:15]=[C:16]([CH2:20][CH2:21][NH:22]C(=O)OC(C)(C)C)[CH:17]=[CH:18][CH:19]=3)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2.Cl>O1CCOCC1>[C:1]12([CH2:11][CH2:12][O:13][C:14]3[CH:15]=[C:16]([CH2:20][CH2:21][NH2:22])[CH:17]=[CH:18][CH:19]=3)[CH2:10][CH:5]3[CH2:6][CH:7]([CH2:9][CH:3]([CH2:4]3)[CH2:2]1)[CH2:8]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 86649160Tert-butyl (2-{3-[2-(1-adamantyl)ethoxy]phenyl}ethyl)-carbamate

생성물 1

HCID 67520349(2-{3-[2-(1-Adamantyl)ethoxy]phenyl}ethyl)amine

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

To a solution of Intermediate 30 (7 g, 17.5 mmol) in dioxane (70 mL) was added hydrogen chloride (1.25M in dioxane, 25 mL). The reaction mixture was stirred at room temperature overnight. The precipitate was filtrated and washed with dioxane and ether. The crude was purified by column chromatography with silica gel, eluting with methylen chloride/methanol/ammonium (40:4:0.2) and the title compound was obtained as an oil (2.6 g, 50%). (M+): 300.

후처리

  1. filtrationThe precipitate was filtrated
  2. washwashed with dioxane and ether
  3. customThe crude was purified by column chromatography with silica gel
  4. washeluting with methylen chloride/methanol/ammonium (40:4:0.2)

출처 및 근거

ORD 기록
ord-2a95a74d120e4f67840889e577092058
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178679B2

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