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

HRID 508846

반응식

HRID 508846 반응식
[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]

참가 물질

4

반응물 2

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

생성물 1

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

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-8129dc9bf9414d85ab2fde8fefb8eff5
출처 데이터셋
uspto-grants-2015_08
특허 번호
US09096545B2

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