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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867171Generated: November 1, 2026

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

https://huagongshe.com/reaction/867171

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 5B 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 (5C), as a yellow liquid, boiling point not determined.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04103021
Source datasetuspto-grants-1978_07
ORD IDord-b670f06f04e546718ed449c6b49d6660
Source noteuspto-grants-1978_07