Cyclohexylammonium Ion → HCID 20394469, compound

HRID 261526Notes

Reaction equation

HRID 261526 reaction equation
[CH2:1]([C:3]1([CH3:18])[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:12](O)([CH3:16])[C:13]([OH:15])=[O:14])[CH:9]=2)[CH2:4]1)[CH3:2].C1([NH3+])CCCCC1>>[CH2:1]([C:3]1([CH3:18])[CH2:11][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([CH:12]([CH3:16])[C:13]([OH:15])=[O:14])[CH:9]=2)[CH2:4]1)[CH3:2]

Participants

3

Reactant 2

HCID 1549093Cyclohexylammonium IonHCID 20394421HCID 20394421, compound

Product 1

HCID 20394469HCID 20394469, compound

Procedure

2-ethyl-α-hydroxy-2,α-dimethyl-5-indanacetic acid is hydrogenated in a manner analogous to that described in Example 1. The cyclohexyl-ammonium salt of the title compound has a M.P. of 165°-167° (from ether).

Sources & evidence

ORD record
ord-2333cdba4d634f6ca10e8be2a54bcc0a
Source dataset
uspto-grants-1979_08
Patent number
US04166131

Reaction notes

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