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2-Naphthalenecarboxamide → Naphthalene-2-carbothioamide

HRID 619343
ノート
印刷プレビュー

反応式

HRID 619343 の反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]([NH2:13])=O.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:23])=CC=1>O1CCCC1>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11](=[S:23])[NH2:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 752452-NaphthalenecarboxamideHCID 87949Lawesson's reagent

生成物 1

HCID 2800333Naphthalene-2-carbothioamide収率 83%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of the above amide (10.0 g, 58 mmol) in dry tetrahydrofuran (250 ml) was added [2,4-bis-(4-methoxyphenyl)-1,3-dithia-2,4-diphosphenate-2,4-disulfide] (Lawesson's reagent) (16.5 g, 41 mmol) and the resulting mixture was stirred at room temperature for 48 h. The volatiles were evaporated in vacuo and the residue was dissolved in ethyl acetate (100 ml) and filtered through silicagel (100 ml) using ethyl acetate as eluent. The solvent was evaporated in vacuo and to the residue was added a mixture of ethyl acetate (25 ml) and heptane (25 ml). The precipitate was filtered off and washed with heptane (40 ml), dried in vacuo at 50° C. which afforded 9.0 g (83%) of naphthalene-2-carbothioic acid amide as a solid.

後処理

  1. customThe volatiles were evaporated in vacuo
  2. dissolutionthe residue was dissolved in ethyl acetate (100 ml)
  3. filtrationfiltered through silicagel (100 ml)
  4. customThe solvent was evaporated in vacuo and to the residue
  5. additionwas added
  6. additiona mixture of ethyl acetate (25 ml) and heptane (25 ml)
  7. filtrationThe precipitate was filtered off
  8. washwashed with heptane (40 ml)
  9. customdried in vacuo at 50° C. which

出典と根拠

ORDレコード
ord-b06feb88ac974582be157603fd178ad2
出典データセット
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05958957

反応ノート

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