HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917915Generated: November 3, 2026
Triethylene Glycol → HCID 21524265, compound
https://huagongshe.com/reaction/917915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylene Glycol | HCID 8172 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 21524257 | HCID 21524257 | — |
| Product | HCID 21524265 | HCID 21524265 | — |
Reaction Steps
A mixture of 12 g of l-methyl-4-oxo-6-cyclohexyl-1,2,3,4-tetrahydronaphthalene-1 -carboxylic acid, 10 g of hydrazine hydrate, 13.7 g of potassium hydroxide, and 85 ml of triethylene glycol is heated at 130°-140°C for 2 hours. After that, while distilling off a mixture of hydrazine and water, the temperature is raised up to 195°C, and the batch is stirred until the evolution of nitrogen ceases. The mixture is then diluted with 50 ml of water, acidified with concentrated hydrochloric acid, then extracted with ethyl acetate. The resin-like crude product remaining after evaporation of the ethyl acetate is crystallized from toluene and yields 1-methyl-6-cyclohexyl-1,2,3,4-tetrahydronaphthalene-1carboxylic acid of the formula ##SPC12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03968142 |
|---|
| Source dataset | uspto-grants-1976_07 |
|---|
| ORD ID | ord-e22b80126362400cb2777cfed897a76d |
|---|
| Source note | uspto-grants-1976_07 |
|---|