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Diethyl Ether → HCID 86680491、化合物

HRID 1497471
ノート
印刷プレビュー

反応式

HRID 1497471 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:12][C:11]([CH:13]=[O:14])=[N:10][N:9]=2)=[CH:4][CH:3]=1.[CH2:15]([Mg]Br)[CH3:16].C(OCC)C>C1COCC1>[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[S:12][C:11]([CH:13]([OH:14])[CH2:15][CH3:16])=[N:10][N:9]=2)=[CH:6][CH:7]=1
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 3

HCID 3283Diethyl EtherHCID 218062345-Formyl-2-(4-fluorophenyl)-1,3,4-thiadiazoleHCID 178418443HCID 178418443、化合物

生成物 1

HCID 86680491HCID 86680491、化合物収率 45%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 5-(4-fluorophenyl)-1,3,4-thiadiazole-2-carbaldehyde (0.2 g, 0.96 mmol) in THF (8 mL) was added 3.0 M solution of ethyl magnesium bromide in diethyl ether (0.96 mL, 2.9 mmol) at 0° C. The reaction mixture was allowed to warm to room temperature and was stirred for 2 h. The reaction mixture was quenched with saturated ammonium chloride solution (15 mL) and water (15 mL), and extracted with ethyl acetate (100 mL). The organic extracts were dried over sodium sulphate and concentrated under reduced pressure to afford 1-(5-(4-fluorophenyl)-1,3,4-thiadiazol-2-yl)propan-1-ol as a yellow solid (0.10 g, 45% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.0-8.03 (m, 1H), 7.39-7.35 (m, 2H), 6.36 (d, 1H), 4.92-4.89 (m, 1H), 1.89-1.78 (m, 2H), 0.95 (t, 3H); LC-MS m/z calcd for [M+H]+ 239.06. found 239.1.

後処理

  1. customThe reaction mixture was quenched with saturated ammonium chloride solution (15 mL) and water (15 mL)
  2. extractionextracted with ethyl acetate (100 mL)
  3. dry with materialThe organic extracts were dried over sodium sulphate
  4. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-aeb1b27a63754118966f32a2e7997b4d
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09199975B2

反応ノート

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