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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893075Generated: October 30, 2026

Hydrochloric Acid → HCID 178439008, compound

https://huagongshe.com/reaction/1893075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantRed-AlHCID 16684438—
Reactant4-{4-[2-(4-Propyl-cyclohexyl)-ethyl]-phenyl}-cyclohexane carboxylic acid methyl esterHCID 58453212—
SolventTolueneHCID 1140—
ProductHCID 178439008HCID 17843900845%

Reaction Conditions

Temperature-40 °C

Reaction Steps

Vitride (3.3M in toluene, 19 mL, 62.7 mmol) was added with syringe to a flask filled with Argon gas, adjusted to 0° C., and morpholine (5.5 ml, 62.7 mmol) was added slowly dropwise with syringe. Then, toluene (31 ml) was added dropwise with syringe to produce vitride solution. 63 ml of a solution including 4-{4-[2-(4-propyl-cyclohexyl)-ethyl]-phenyl}-cyclohexane carboxylic acid methyl ester (2.3 g, 6.27 mmol) obtained in Example 5-2 in toluene a solution was added to another flask filled with argon gas, and vitride solution was added slowly dropwise at −70° C. for 30 minutes. Then, the solution was stirred with maintaining −30 to −50° C. for 6 hours and water was added very slowly dropwise to the flask. After reaction, 1M HCl was slowly added to the flask to neutralize the reaction solution. White precipitate was filtered under reduced pressure and the filtrate was extracted by toluene (20 ml×three times). The organic layer was collected, washed by distilled water (10 ml×two times), dried with anhydrous Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by column chromatography (hexane:ether=5:1, Rf=0.32) to produce 0.96 g (45%) of trans-4-{4-[2-(4-propyl-cyclohexyl)ethyl]phenyl}cyclohexane carbaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08512598B2
Source datasetuspto-grants-2013_08
ORD IDord-44ff6e8de08442d7b0cdcb0f01c15561
Source noteuspto-grants-2013_08