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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 371063Generated: October 30, 2026

Pyridine → Tricyclo(3.3.1.13,7)decane-1-carboxylic acid, (3-phenoxyphenyl)methyl

https://huagongshe.com/reaction/371063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-Phenoxybenzyl alcoholHCID 26295—
Reactant1-Adamantanecarbonyl chlorideHCID 98915—
SolventBenzeneHCID 241—
ProductTricyclo(3.3.1.13,7)decane-1-carboxylic acid, (3-phenoxyphenyl)methylHCID 18523998.7%

Reaction Steps

1 g (5.03 mmol) of tricyclo[3.3.1.13,7 ]decane-1-carbonyl chloride, 1.01 g (5.04 mmol) of 3-phenoxybenzyl alcohol and 0.08 g (10.07 mmol) of anhydrous pyridine were dissolved in 30 ml of anhydrous benzene. The mixture was stirred at room temperature for 66 hours. Then the reaction was terminated. The resulting pyridine hydrochloride was removed by filtration and the filtrate was thoroughly washed with 1N hydrochloric acid, 5% sodium carbonate and then saturated saline solution, and dried over sodium sulfate. The solvent was removed to obtain 1.8 g of an oily material. Purification by column chromatography on silica gel employing a developer consisting of n-hexane and benzene (1:1) gave 1.69 g (yield 93%) of a colorless oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04529599
Source datasetuspto-grants-1985_07
ORD IDord-cd3cfd4fb4ff45c3a5b930badd7a7106
Source noteuspto-grants-1985_07