Oxalyl chloride → HCID 12534981、化合物
反応式
[C:1](Cl)(=O)[C:2]([Cl:4])=[O:3].[CH2:7]([C:12]12[CH2:19][CH2:18]C(C(O)=O)([CH2:16][CH2:17]1)[CH2:14][CH2:13]2)[CH2:8][CH2:9][CH2:10][CH3:11]>C(Cl)Cl>[CH2:7]([C:12]12[CH2:19][CH2:18][C:1]([C:2]([Cl:4])=[O:3])([CH2:14][CH2:13]1)[CH2:16][CH2:17]2)[CH2:8][CH2:9][CH2:10][CH3:11]参加物
4
実験手順
Oxalyl chloride (505 μL, 5.79 mmol) was added dropwise to a mixture of 4-pentylbicyclo[2.2.2]octane-1-carboxylic acid (3-A) in methylene chloride (10 mL). The solution was stirred at room temperature for 3 h and then concentrated in vacuo to give 4-pentylbicyclo[2.2.2]octane-1-carbonyl chloride (3-B). 1H NMR (500 MHz, CDCl3): δ 0.90 (t, 3H); 1.21 (m, 8H); 1.45 (m, 6H); 1.88 (m, 6H) ppm.
後処理
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-9bd2011406074f07adcdcd4b944ef2be
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06849636B2
反応ノート
読み込み中…