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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447792Generated: October 30, 2026

methyl 6-chloro-2H-chromene-3-carboxylate → Methyl 6-chloro-3,4-dihydro-2H-1-benzopyran-3-carboxylate

https://huagongshe.com/reaction/1447792

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 6-chloro-2H-chromene-3-carboxylateHCID 2763891—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductMethyl 6-chloro-3,4-dihydro-2H-1-benzopyran-3-carboxylateHCID 20383065—

Reaction Steps

700 mg of 6B was dissolved in 75 ml of ethyl acetate and the solution was treated with hydrogen (initial pressure of 30 psig), in the presence of a 10% palladium-on-carbon catalyst, for 8 hours. The reaction mixture then was filtered and stripped of solvent to give methyl 6-chloro-3,4-dihydro-2H-1-benzopyran-3-carboxylate (6C), as a yellow liquid, boiling point not determined.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04178380
Source datasetuspto-grants-1979_12
ORD IDord-48dc98b57d864474931373062465d6e6
Source noteuspto-grants-1979_12