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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991923Generated: October 31, 2026

Carbon Dioxide → Adapalene

https://huagongshe.com/reaction/1991923

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantSodium hydrideHCID 24758—
Reactant6-[3-(1-Adamantyl)-4-methoxyphenyl]-2-bromonaphthaleneHCID 59129802—
ReactantHCID 178418306HCID 178418306—
SolventHydrochloric AcidHCID 313—
SolventTetrahydrofuranHCID 8028—
ProductAdapaleneHCID 60164—

Reaction Conditions

Temperature-60 °C

Reaction Steps

A mixture of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2-bromonaphthalene (50 mg, 0.11 mmol) in THF (1 ml) was introduced into a Schlenk tube and was heated until its complete dissolution. Next, NaH (4.5 mg, 60% dispersion in mineral oil, 0.11 mmol) was added under argon atmosphere and at room temperature, and the mixture was stirred for 10 minutes. The obtained mixture was cooled to −60° C. and t-BuLi (1.7 M in penthane, 0.22 mmol) was added, dropwise, during a period of 30 minutes. Next, and at the same temperature, a continuous mild flow of CO2 (anhydrous gas) was introduced in the reaction for 1 h. After bringing the reaction to room temperature during 30 minutes with continuous flow of CO2, the mixture was diluted with aq HCl (5 ml, 2 M) and was vigorously stirred for 10 minutes. The resulting mixture was extracted with CHCl3 (3×5 ml) and the joined organic phases were evaporated to dryness once dried with Na2SO4, giving the crude of Adapalene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645910B2
Source datasetuspto-grants-2010_01
ORD IDord-82640073440548fb9ce8d7384318251c
Source noteuspto-grants-2010_01