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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398909Generated: October 30, 2026

7-(3-cyclopropyl-2-propyl)-1,2-dihydro9-hydroxy-4-oxo-4H-thieno[2,3-c][1]benzopyran → 7-(3-cyclopropyl-2-propyl)-4,4-di(1-hexyl)-1,2-dihydro-9-hydroxy-4H-thieno[2,3-c][1]benzopyran

https://huagongshe.com/reaction/2398909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-(3-cyclopropyl-2-propyl)-1,2-dihydro9-hydroxy-4-oxo-4H-thieno[2,3-c][1]benzopyranHCID 21433870—
ReactantHCID 178444609HCID 178444609—
Product7-(3-cyclopropyl-2-propyl)-4,4-di(1-hexyl)-1,2-dihydro-9-hydroxy-4H-thieno[2,3-c][1]benzopyranHCID 21433890—

Reaction Steps

By reacting 7-(3-cyclopropyl-2-propyl)-1,2-dihydro9-hydroxy-4-oxo-4H-thieno[2,3-c][1]benzopyran with n-hexyl magnesium bromide, using the procedure described above in Example 8, there is obtained 7-(3-cyclopropyl-2-propyl)-4,4-di(1-hexyl)-1,2-dihydro-9-hydroxy-4H-thieno[2,3-c][1]benzopyran. The benzopyran is then reacted with morpholinoacetic acid and dicyclohexylcarbodiimide according to the method of Example 9 to yield the desired ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04025630
Source datasetuspto-grants-1977_05
ORD IDord-fa4424b61590493aaeb84c8f4b032e11
Source noteuspto-grants-1977_05