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4-(Trifluoromethyl)benzoic acid → Benzoic acid, 4-(trifluoromethyl)-, sodium salt (1:1)

HRID 490704
ノート
印刷プレビュー

反応式

HRID 490704 の反応式
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=[O:8])=[CH:5][CH:4]=1.[OH-].[Na+:15]>CO>[F:1][C:2]([F:12])([F:13])[C:3]1[CH:11]=[CH:10][C:6]([C:7]([O-:9])=[O:8])=[CH:5][CH:4]=1.[Na+:15]
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 99664-(Trifluoromethyl)benzoic acidHCID 14798Sodium Hydroxide

生成物 1

HCID 23717385Benzoic acid, 4-(trifluoromethyl)-, sodium salt (1:1)

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a solution of 4-trifluoromethyl benzoic acid (0.100 g, 0.239 mmole) in methanol (2.0 mL), is added sodium hydroxide (0.093 g, 0.287 mmole) and stirred at room temperature for 2 hours. The mixture is concentrated to dryness in vacuo to give sodium 4-trifluoromethyl-benzoate as a white solid. It is then mixed with NH4OAc (8.32 g, 107.9 mmole) in glacial acetic acid (500 mL) and heated at 100° C. for 16 hours. After removed the solvents on rota-vapor, the residue is partitioned between ethyl acetate (300 mL) and saturated sodium bicarbonate (300 mL). Extracted the aqueous layer with ethyl acetate (300 mL) one more time. The combined organic is wash with brine (3×500 mL), dried over Na2SO4, filtered and concentrated. The crude product is purified by chromatography on silica gel column, gradient elute with 0 to 10% ethyl acetate in hexane and concentrated to provide the titled compound as a white solid. Mass [EI+] 300 (M++H).

後処理

  1. concentrationThe mixture is concentrated to dryness in vacuo

出典と根拠

ORDレコード
ord-083583a5a03f439f881cb08b9283fbb8
出典データセット
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07528160B2

反応ノート

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