Hydrochloric Acid → Acetic acid, 2-[[2-(1,1-dimethylethyl)phenyl]amino]-2-oxo-

HRID 350624

反応式

HRID 350624 の反応式
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[NH:11][C:12](=[O:17])[C:13]([O:15]C)=[O:14])([CH3:4])([CH3:3])[CH3:2].CO.[OH-].[Na+].CO.Cl>O>[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[NH:11][C:12](=[O:17])[C:13]([OH:15])=[O:14])([CH3:4])([CH3:2])[CH3:3]

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 11183932Methyl 2-((2-(tert-butyl)phenyl)amino)-2-oxoacetateHCID 23721981Sodium hydroxide methanol

生成物 1

HCID 11550317Acetic acid, 2-[[2-(1,1-dimethylethyl)phenyl]amino]-2-oxo-

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A 3-L, 3-necked round-bottomed flask, equipped with a mechanic stirrer and a thermal probe (under nitrogen) was charged with Methyl 2-(2-tert-Butylphenylamino)-2-oxoacetate (154 g, 655 mmoles) and MeOH (1000 mL). The resulting mixture was stirred at a moderate speed at room temperature. A solution of 1N NaOH/MeOH (800 mL) was added dropwise to the reaction mixture via addition funnel. After 1 hour, agitation was stopped, and the suspension transferred to a filtration funnel and filtered to afford a white solid. This solid was then taken up in water (1200 mL) and the pH adjusted to 1.5–2 with addition of conc. HCl with stirring. After mixing for 1 hour, filtration and drying yielded the title compound as a white crystalline mass (127 g, 574 mmoles, 87.6%). TLC (silica F254, 3/1 v/v dichloromethane/MeOH, detection 254 nm) showed one spot and HPLC confirmed that. MP 110.9–112.6° C.; IR (KBr) 3405, 2973, 1688, 1548, 1300, 757 cm−1; 1H NMR (300 MHz, CDCl3): δ (ppm): 9.37 (br, 1H), 7.91 (dd, J=7.8 Hz, J′=1.8 Hz, 1H), 7.44 (dd, J=7.8 Hz, J′=1.8 Hz, 1H), 7.25 (m, 2H), 1.46 (s, 9H); 13C (300 MHz, CDCl3): δ (ppm): 160.87, 155.24, 141.18, 133.19, 126.92, 126.69, 126.63, 124.24, 34.21, 30.49.

後処理

  1. customthe suspension transferred to a filtration funnel
  2. filtrationfiltered
  3. customto afford a white solid
  4. stirringwith stirring
  5. additionAfter mixing for 1 hour
  6. filtrationfiltration
  7. customdrying

出典と根拠

ORDレコード
ord-10fb17fd794a4c3d932601692fb4d65a
出典データセット
uspto-grants-2007_02
特許番号
US07183260B2

関連ノート

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