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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346285Generated: October 29, 2026

Benzocaine → N-(4-carbethoxyphenyl)-1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-2-aminoethanol

https://huagongshe.com/reaction/346285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzocaineHCID 2337—
Reactant(5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)oxiraneHCID 14726539—
SolventTolueneHCID 1140—
ProductN-(4-carbethoxyphenyl)-1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-2-aminoethanolHCID 1472654030.9%

Reaction Steps

26 g (110 millimoles) of (5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-oxirane, 15 g (90 millimoles) of ethyl 4-aminobenzoate, 135 g of basic alumina and 450 ml of toluene were refluxed for 2 hours. The solid was then filtered off and the filtrate was evaporated down. After recrystallization from n-heptane with a little ethyl acetate, the residue gave 11.0 g of N-(4-carbethoxyphenyl)-1-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-2-aminoethanol. The structure was determined by H-NMR spectroscopy. 3-(4-Carbethoxyphenyl)-5-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)-oxazolidine:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05061705
Source datasetuspto-grants-1991_10
ORD IDord-828cf23b3459402eb9332ebcb1d2b72c
Source noteuspto-grants-1991_10