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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917908Generated: November 1, 2026

Potassium Hydroxide → 1-Methyl-6-cyclohexyl-7-chloro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid

https://huagongshe.com/reaction/917908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1-Methyl-4-oxo-6-cyclohexyl-7-chloro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acidHCID 21524254—
SolventTriethylene GlycolHCID 8172—
Product1-Methyl-6-cyclohexyl-7-chloro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acidHCID 2152425692.1%

Reaction Conditions

Temperature195 °C

Reaction Steps

A mixture of 6.7 g of 1-methyl-4-oxo-6-cyclohexyl-7-chloro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid, 4 g of hydrazine hydrate, 6.7 g of potassium hydroxide and 40 ml of triethyleneglycol is heated for 2 hours at 130°-140°C. Then, while distilling off a mixture of hydrazine and water, the temperature is raised to 195°C and the batch is stirred until nitrogen is no longer being given off, then diluted with 50 ml of water, acidified with concentrated hydrochloric acid and the mixture is extracted with ethyl acetate. The ethyl acetate is evaporated and the residual crude product recrystallized from acetone, to yield 5.9 g of 1-methyl-6-cyclohexyl-7-chloro-1,2,3,4-tetrahydronaphthalene-1-carboxylic acid melting at 167°-168°C, of the formula ##SPC7##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03968142
Source datasetuspto-grants-1976_07
ORD IDord-cdf5fd5d8d2a4b30b971afb67ac6d4cc
Source noteuspto-grants-1976_07