반응 #437806

ord-10fb17fd794a4c3d932601692fb4d65a

반응 방정식

CO.[Na+].[OH-]
NaOH MeOH
COC(=O)C(=O)Nc1ccccc1C(C)(C)C
Methyl 2-(2-tert-Butylphenylamino)-2-oxoacetate
CO
MeOH
Cl
HCl
CC(C)(C)c1ccccc1NC(=O)C(=O)O
title compound
CC(C)(C)c1ccccc1NC(=O)C(=O)O
2-(2-tert-Butyl phenylamino)-2-oxoacetic acid

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the suspension transferred to a filtration funnel
  2. 2
    여과filtered
  3. 3
    기타to afford a white solid
  4. 4
    workup.STIRRINGwith stirring
  5. 5
    workup.ADDITIONAfter mixing for 1 hour
  6. 6
    여과filtration
  7. 7
    기타drying

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07183260B2uspto-grants-2007_02