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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581079Generated: November 1, 2026

5-Hydroxy-2-tetralone → 1,2,3,4-Tetrahydro-5-[2,3-epoxy-propoxy]-2-naphthol

https://huagongshe.com/reaction/1581079

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Hydroxy-2-tetraloneHCID 5103527—
Reactant5,6,7,8-Tetrahydronaphthalene-1,6-diolHCID 12445738—
ReactantNaphthalen-1(2H)-oneHCID 12446728—
Product1,2,3,4-Tetrahydro-5-[2,3-epoxy-propoxy]-2-naphtholHCID 12445767—

Reaction Steps

Employing the procedure of Example 3 a, but substituting a 6-alkoxy-1-tetralone as shown in the left hand (first) column of Table II for 6-methoxy-1-tetralone, a 6-alkoxy-1-naphthol is produced, which is converted as per Example 3 b to the corresponding 5-hydroxy-3,4-dihydro-2(1H)-naphthalenone shown in the middle column of Table II; employing the procedure of Example 3 c the naphthalenone is converted to the corresponding 5,6,7,8-tetrahydro-1,6-naphthalenediol which is reacted with an epoxide of the structure ##EQU13## in accordance with the procedure of Example 3d to form the corresponding 1,2,3,4-tetrahydro-5-[2,3-epoxy-propoxy]-2-naphthol which is reacted with an amine of the structure ##EQU14## in accordance with the procedure of Example 3e to form the corresponding 1,2,3,4-tetrahydro-5-[2-hydroxy-3-(R1, R2 -substituted amino)propoxy]-2-naphthol (formula I) as shown in the right hand (third) column of Table II.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03935267
Source datasetuspto-grants-1976_01
ORD IDord-d4200412419642b3ad73963a3a43e8ab
Source noteuspto-grants-1976_01