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Hydrochloric Acid → 6-Fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochloride

HRID 1592335
ノート
印刷プレビュー

反応式

HRID 1592335 の反応式
[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH2:8][C:7](=[N:12]O)[CH2:6][CH2:5]2.[ClH:14]>[Pd].CO>[ClH:14].[F:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH2:8][CH:7]([NH2:12])[CH2:6][CH2:5]2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 313Hydrochloric AcidHCID 860515846-fluoro-3,4-dihydronaphthalen-2(1H)-one Oxime

生成物 1

HCID 196993636-Fluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamine hydrochloride収率 83%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A mixture of 6-fluoro-3,4-dihydronaphthalen-2(1H)-one oxime (1.58 g, 8.81 mmol), methanol (25 mL), conentrated hydrochloric acid (2 mL) and 10% palladium on charcoal (316 mg) was shaken in a pressure bottle under a hydrogen atmosphere (55 psig). After 18 hours, the mixture was filtered and the solid washed with methanol. The filtrate was concentrated under vacuum, and the residue was washed with ether, dried by concentration from benzene, and dried further under vacuum to provide a white solid (1.48 g, 83%).

後処理

  1. filtrationthe mixture was filtered
  2. washthe solid washed with methanol
  3. concentrationThe filtrate was concentrated under vacuum
  4. washthe residue was washed with ether
  5. dry with materialdried by concentration from benzene
  6. customdried further under vacuum

出典と根拠

ORDレコード
ord-585afe5e44ee4a9c8b76bd8f4bd5ae18
出典データセット
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07291744B2

反応ノート

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