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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282849Generated: October 29, 2026

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

https://huagongshe.com/reaction/1282849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-dihydro-9-hydroxy-7-methyl-4-oxo-4H-thieno[2,3-c][1]benzopyranHCID 21433872—
ReactantHCID 178444609HCID 178444609—
Product4,4-di(1-hexyl)-1,2-dihydro-9-hydroxy-7-methyl-4H-thieno[2,3-c][1]benzopyranHCID 21433881—

Reaction Steps

By reacting 1,2-dihydro-9-hydroxy-7-methyl-4-oxo-4H-thieno[2,3-c] [1]benzopyran with n-hexyl magnesium bromide, using the procedure described in Example 8, there is obtained 4,4-di(1-hexyl)-1,2-dihydro-9-hydroxy-7-methyl-4H-thieno [2,3-c] [1]benzopyran. The benzopyran is then reacted with γ-pyrrolidinobutyric acid, hydrobromide salt and dicyclohexylcarbodiimide according to the method of Example 10 to yield the desired ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03972880
Source datasetuspto-grants-1976_08
ORD IDord-ed5fd7027cdc4154ad93abd502555f82
Source noteuspto-grants-1976_08