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Hydrochloric Acid → alpha,alpha-Dimethyl-2-naphthaleneethanamine

HRID 895873
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인쇄 미리보기

반응식

HRID 895873 반응식
[CH3:1][C:2]([NH:15]C(=O)C)([CH3:14])[CH2:3][C:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=1.Cl.[OH-].[Na+]>O>[CH3:14][C:2]([NH2:15])([CH3:1])[CH2:3][C:4]1[CH:13]=[CH:12][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 22382419N-[2-Methyl-1-(naphthalen-2-yl)propan-2-yl]acetamide

생성물 1

HCID 15369616alpha,alpha-Dimethyl-2-naphthaleneethanamine수율 88.5%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To N-[2-methyl-1-(naphthalen-2-yl)propan-2-yl]acetamide (26 mg) obtained in Step 8 was added 6N hydrochloric acid (2 ml) and the mixture was heated under reflux for 5 hr. The reaction mixture was poured into water, made basic with a 4N aqueous sodium hydroxide solution, and extracted with diethyl ether. The organic layer was washed with water, dried over potassium carbonate and concentrated under reduced pressure to give the title compound (19 mg).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 5 hr
  3. extractionextracted with diethyl ether
  4. washThe organic layer was washed with water
  5. dry with materialdried over potassium carbonate
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-8d1a65d1e9f44f4cb61297243c0c3a2c
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06916956B2

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