4-Bromo-2-furaldehyde → (Z)-4-(prop-1-enyl)furan-2-carbaldehyde

HRID 2105559

反応式

HRID 2105559 の反応式
Br[C:2]1[CH:3]=[C:4]([CH:7]=[O:8])[O:5][CH:6]=1.[CH:9](/B(O)O)=[CH:10]/[CH3:11].C(C1OC(C=O)=CC=1)C1C=CC=CC=1>CN(C=O)C>[CH:9](/[C:2]1[CH:3]=[C:4]([CH:7]=[O:8])[O:5][CH:6]=1)=[CH:10]/[CH3:11]

参加物

5

反応物 3

HCID 27570104-Bromo-2-furaldehydeHCID 5355539(Z)-Prop-1-en-1-ylboronic acidHCID 124185375-Benzylfuran-2-carbaldehyde

生成物 1

HCID 59648561(Z)-4-(prop-1-enyl)furan-2-carbaldehyde収率 48.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

The title compound was synthesized from 4-bromo-furan-2-carboxaldehyde (1.1 g, 6.3 mmol, 1 equiv) and cis-propene boronic acid (0.65 g, 7.5 mmol, 1.2 equiv) using the conditions to synthesize 5-benzyl-furan-2-carbaldehyde, with the exception that the reaction was run in DMF (20 mL). The resulting residue was purified via ISCO Companion (0-25% EtOAc/heptane over 30 min, retention time of product: 23-26 min) to give (Z)-4-(prop-1-enyl)furan-2-carbaldehyde (0.4130 g, 48% yield). LC/MS m/e 136.8 (M+H). 1H NMR (400 MHz, CD3CN) δ (ppm): 9.59 (d, J=0.63 Hz, 1 H), 7.83 (s, 1 H), 7.42 (s, 1 H), 6.23 (dd, J=11.40, 1.68 Hz, 1 H), 5.79-5.89 (m, 1 H), 1.87 (dd, J=7.10, 1.78 Hz, 3 H).

後処理

  1. customThe resulting residue was purified via ISCO Companion (0-25% EtOAc/heptane over 30 min, retention time of product: 23-26 min)

出典と根拠

ORDレコード
ord-2e2d6d2943bd48e38a8a6c40c90d773a
出典データセット
uspto-grants-2009_08
特許番号
US07579370B2

関連ノート

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