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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 28401656, 화합물

HRID 2167469
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HRID 2167469 반응식
Cl.[Br:2][C:3]1[CH:4]=[CH:5][C:6]([O:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:7]([NH:9]C(=O)C)[CH:8]=1.[OH-].[Na+]>C(O)C>[Br:2][C:3]1[CH:4]=[CH:5][C:6]([O:13][CH:14]2[CH2:18][CH2:17][CH2:16][CH2:15]2)=[C:7]([CH:8]=1)[NH2:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 66917186HCID 66917186, 화합물

생성물 1

HCID 28401656HCID 28401656, 화합물수율 101.7%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Concentrated hydrochloric acid (5.8 ml) was added to an ethanol solution (100 ml) of N-(5-bromo-2-cyclopentyloxyphenyl)acetamide (3.4 g, 11.4 mmol), and the resulting mixture was stirred for 3 hours while heating under reflux. After the reaction mixture was cooled to room temperature, a 5N sodium hydroxide solution (14.2 ml) was added to obtain a pH of 11. The resulting mixture was then extracted with dichloromethane. The organic layer was washed with a saturated sodium chloride aqueous solution, and then concentrated under reduced pressure. The residue was then purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1). The purified product was concentrated under reduced pressure to thereby obtain 2.97 g of oily pale yellow 5-bromo-2-cyclopentyloxyaniline (yield: 100%).

후처리

  1. temperaturewhile heating
  2. temperatureunder reflux
  3. customto obtain a pH of 11
  4. extractionThe resulting mixture was then extracted with dichloromethane
  5. washThe organic layer was washed with a saturated sodium chloride aqueous solution
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was then purified by silica gel column chromatography (n-hexane:ethyl acetate=4:1)
  8. concentrationThe purified product was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-68dcedbc172847a59334ce9b858cc20d
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09045464B2

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