Sulfuric Acid → HCID 59139223, compound

HRID 599824Notes

Reaction equation

HRID 599824 reaction equation
S(=O)(=O)(O)O.[C:6]1([CH:13]=[CH:12][CH:11]=[C:9]([OH:10])[CH:8]=1)[OH:7].C([O:16][C:17](=O)[CH:18]([CH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([N+:29]([O-:31])=[O:30])[C:24]=1[F:32])[C:19](=O)[CH3:20])C>O>[F:32][C:24]1[C:25]([N+:29]([O-:31])=[O:30])=[CH:26][CH:27]=[CH:28][C:23]=1[CH2:22][C:18]1[C:17](=[O:16])[O:7][C:6]2[CH:8]=[C:9]([OH:10])[CH:11]=[CH:12][C:13]=2[C:19]=1[CH3:20]

Participants

5

Reactant 3

HCID 1118Sulfuric AcidHCID 5054ResorcinolHCID 58232217HCID 58232217, compound

Product 1

HCID 59139223HCID 59139223, compoundYield 64%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Concentrated sulfuric acid (21.5 mL) was added at 0° C. to a mixture of resorcinol (14.8 g, 135 mmol) and 2-(2-fluoro-3-nitrobenzyl)-3-oxobutanoic acid ethyl ester (38.2 g, 135 mmol), and the reaction mixture was stirred at room temperature overnight. The reaction mixture was then poured into water, and the solid was filtered off. It was washed with water and methanol to yield the title compound (28.3 g, 64%) as a pale yellow powder.

Workup

  1. filtrationthe solid was filtered off
  2. washIt was washed with water and methanol

Sources & evidence

ORD record
ord-3f367eb85d5d4ac0bd8e832669649fc6
Source dataset
uspto-grants-2011_03
Patent number
US07897792B2

Reaction notes

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