Oxalyl chloride → HCID 14501734、化合物
反応式
[C:1]([Cl:6])(=[O:5])[C:2](Cl)=[O:3].[F:7][C:8]([F:16])([F:15])[CH2:9]OCC(O)=O>ClCCl.CN(C)C=O>[F:7][C:8]([F:16])([F:15])[CH2:9][O:3][CH2:2][C:1]([Cl:6])=[O:5]参加物
実験手順
A solution of oxalyl chloride (20 mL, 0.23 mol, 1.15 eq) in dry dichloromethane (50 mL) was added dropwise at room temperature, with stirring, to a solution of (2,2,2-trifluoroethoxy)ethanoic acid (int. Patent Appl., Publication No. WO 87/07270, 31.6 g, 0.2 mol) and N,N-dimethylformamide (5 drops) in dry dichloromethane (400 mL). The mixture was stirred for an additional hour, then heated under reflux for 2 hours, cooled and the bulk of the solvent removed by distillation (bp 40-45° C./760 mm Hg). The residue was transferred to a Claisen distillation flask and the remaining solvent and oxalyl chloride removed by distillation (bp 45-60° C./760 mm Hg). Vacuum distillation of the residue then afforded the product, bp 50-55°/25-32 mm Hg. δH (CDCl3) 4.00 (2H, q, 3JHF 8.3) and 4.57 (2H, s).
後処理
- temperatureheated
- temperatureunder reflux for 2 hours
- temperaturecooled
- customthe bulk of the solvent removed by distillation (bp 40-45° C./760 mm Hg)
- distillationThe residue was transferred to a Claisen distillation flask
- customthe remaining solvent and oxalyl chloride removed by distillation (bp 45-60° C./760 mm Hg)
- distillationVacuum distillation of the residue
- customthen afforded the product, bp 50-55°/25-32 mm Hg
出典と根拠
- ORDレコード
- ord-5a974d909d5d4fd7b7820f92583938eb
- 出典データセット
- uspto-grants-2000_12
- 特許番号
- US06166049
反応ノート
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