2,6-Dimethylbenzoic acid → 2,6-Dimethyl-3-((2,2,2-trifluoroacetamido)methyl)benzoic acid

HRID 59353

反応式

HRID 59353 の反応式
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[C:7]([CH3:11])[C:3]=1[C:4]([OH:6])=[O:5].[F:12][C:13]([F:20])([F:19])[C:14]([NH:16][CH2:17]O)=[O:15]>OS(O)(=O)=O>[F:12][C:13]([F:20])([F:19])[C:14]([NH:16][CH2:17][C:10]1[C:2]([CH3:1])=[C:3]([C:7]([CH3:11])=[CH:8][CH:9]=1)[C:4]([OH:6])=[O:5])=[O:15]

参加物

4

反応物 2

HCID 124392,6-Dimethylbenzoic acidHCID 30849312,2,2-Trifluoro-N-(hydroxymethyl)acetamide

生成物 1

HCID 866922272,6-Dimethyl-3-((2,2,2-trifluoroacetamido)methyl)benzoic acid収率 56,519.699%

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

To a solution of 2,6-dimethyl benzoic acid (6.8 g, 0.045 mmol) in conc. H2SO4 (100 mL), 2,2,2-trifluoro-N-(hydroxymethyl)acetamide (7.1 g, 0.049 mmol) was added and the reaction mixture was stirred at RT for 24 h. After completion of the reaction, the reaction mass was quenched in ice water and stirred for 15 minutes. The obtained solid product was filtered and dried to afford 7.0 g of the desired title product. 1H NMR (300 MHz, DMSO d6): δ 2.26 (s, 6H), 4.36 (t, J=12.3 Hz, 2H), 7.09 (m, 1H), 7.15 (m, 1H), 9.89-9.94 (m, 1H).

後処理

  1. customAfter completion of the reaction
  2. customthe reaction mass was quenched in ice water
  3. stirringstirred for 15 minutes
  4. filtrationThe obtained solid product was filtered
  5. customdried

出典と根拠

ORDレコード
ord-c521480019fd45eb94312a773d2c8503
出典データセット
uspto-grants-2016_09
特許番号
US09439890B2

関連ノート

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