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Continuous-Flow Synthesis of Δ9-Tetrahydrocannabinol and Δ8-Tetrahydrocannabinol from Cannabidiol.


ABSTRACT: A challenging step in the preparation of tetrahydrocannabinol analogs is an acid-catalyzed intramolecular cyclization of the cannabidiol precursor. This step typically affords a mixture of products, which requires extensive purification to obtain any pure products. We report the development of two continuous-flow protocols for the preparation of (-)-trans9-tetrahydrocannabinol and (-)-trans8-tetrahydrocannabinol.

SUBMITTER: Bassetti B 

PROVIDER: S-EPMC10167683 | biostudies-literature | 2023 May

REPOSITORIES: biostudies-literature

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Continuous-Flow Synthesis of Δ<sup>9</sup>-Tetrahydrocannabinol and Δ<sup>8</sup>-Tetrahydrocannabinol from Cannabidiol.

Bassetti Benedetta B   Hone Christopher A CA   Kappe C Oliver CO  

The Journal of organic chemistry 20230404 9


A challenging step in the preparation of tetrahydrocannabinol analogs is an acid-catalyzed intramolecular cyclization of the cannabidiol precursor. This step typically affords a mixture of products, which requires extensive purification to obtain any pure products. We report the development of two continuous-flow protocols for the preparation of (-)-<i>trans</i>-Δ<sup>9</sup>-tetrahydrocannabinol and (-)-<i>trans</i>-Δ<sup>8</sup>-tetrahydrocannabinol. ...[more]

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