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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218687Generated: November 3, 2026

5-Benzyloxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid → 5-benzyloxy-N-(4-butylphenyl)-N-[(4-dimethylaminophenyl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamide

https://huagongshe.com/reaction/218687

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Benzyloxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acidHCID 11208318—
Reactant(4-Butylphenyl)[(4-dimethylaminophenyl)methyl]amineHCID 21957943—
Product5-benzyloxy-N-(4-butylphenyl)-N-[(4-dimethylaminophenyl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamideHCID 6718376192%

Reaction Steps

By the reaction and treatment in the same manner as in Example 12 using 5-benzyloxy-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid (0.66 g) and (4-butylphenyl)[(4-dimethylaminophenyl)methyl]amine (0.55 g) as starting materials, 5-benzyloxy-N-(4-butylphenyl)-N-[(4-dimethylaminophenyl)methyl]-1,2,3,4-tetrahydronaphthalene-1-carboxamide (0.98 g) was obtained. By the reaction and treatment in the same manner as in Example 17 using this compound, N-(4-butylphenyl)-N-[(4-dimethylaminophenyl)methyl]-5-hydroxy-1,2,3,4-tetrahydronaphthalene-1-carboxamide (0.44 g) was obtained. melting point: 138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198454B2
Source datasetuspto-grants-2012_06
ORD IDord-2da43d9f3467476fbbaf0f6ca4edbb41
Source noteuspto-grants-2012_06