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2-(6-Methoxy-2-naphthyl)propionic acid → 2-(6-Methoxynaphthalen-2-yl)propanoic acid--ethanamine (1/1)

HRID 1607488
Notes
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Reaction equation

HRID 1607488 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([CH3:17])[C:14]([OH:16])=[O:15])[CH:7]=[CH:6]2.[CH2:18]([NH2:20])[CH3:19]>CC(C)=O>[CH2:18]([NH2:20])[CH3:19].[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([CH3:17])[C:14]([OH:16])=[O:15])[CH:7]=[CH:6]2
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 13022-(6-Methoxy-2-naphthyl)propionic acidHCID 6341Ethylamine

Product 1

HCID 441538962-(6-Methoxynaphthalen-2-yl)propanoic acid--ethanamine (1/1)

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Conditions

Temperature
25 °C

Procedure

230 g (1 mole) of (±)-2-(6-methoxy-2-naphthyl) propionic acid was dissolved in 1.5 l of acetone at about 45° C. By addition of 64 g (1 mole) of a 70% w/w aqueous monoethylamine solution, the ethylamine salt crystallized. The mixture was cooled to about 25° C., filtered and washed portionwise with 200 ml of acetone.

Workup

  1. customthe ethylamine salt crystallized
  2. filtrationfiltered
  3. washwashed portionwise with 200 ml of acetone

Sources & evidence

ORD record
ord-2285ac221bcd47ad96639dd2f910b1c6
Source dataset
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04865770

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes