Acetic Anhydride → HCID 14722248, compound

HRID 1639017Notes

Reaction equation

HRID 1639017 reaction equation
[CH:1]1([N:7]=[C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11](=[O:18])[C:10]([O:19][CH3:20])=[CH:9]2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[C:21](OC(=O)C)(=[O:23])[CH3:22]>>[CH:1]1([NH:7][C:8]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]([O:18][C:21](=[O:23])[CH3:22])=[C:10]([O:19][CH3:20])[CH:9]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

3

Reactant 2

HCID 7918Acetic AnhydrideHCID 14722247HCID 14722247, compound

Product 1

HCID 14722248HCID 14722248, compound

Procedure

A suspension of 4-cyclohexylimino-1-oxo-2-methoxy-1,4-dihydronaphthalene in acetic anhydride is hydrogenated according to the procedure in Example 1 to obtain 4-cyclohexylamino-1-acetoxy-2-methoxynaphthalene, m.p. 134°-136° C.

Sources & evidence

ORD record
ord-b7b4db8903d449a4958556a3421d875d
Source dataset
uspto-grants-1989_11
Patent number
US04882339

Reaction notes

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