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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032489Generated: October 31, 2026

Methanol → 5,6-Dihydroxy-N-methylisoindoline hydrobromide

https://huagongshe.com/reaction/1032489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-benzyl-5,6-dihydroxy-N-methylisoindolinium bromideHCID 14993734—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventAcetic AcidHCID 176—
Product5,6-Dihydroxy-N-methylisoindoline hydrobromideHCID 14098422—

Reaction Steps

1.0 g (2.97 mmol) of N-benzyl-5,6-dihydroxy-N-methylisoindolinium bromide obtained in Example 4 was dissolved in a solution comprising 10 ml of methanol and 10 ml of acetic acid, and 300 mg of a 10% palladium carbon catalyst was added thereto. Then, the catalytic reduction was conducted at 60° C. for 6 hours in a hydrogen gas stream. After filtering off the catalyst, the filtrate was evaporated to dryness under reduced pressure. To the residue, 10 ml of methanol was added, and the mixture was left to cool. The precipitated crystals were collected by filtration and washed with 10 ml of acetone to obtain 500 mg of the above identified compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04958029
Source datasetuspto-grants-1990_09
ORD IDord-1d3cb6fe86164c3e927cd40d5058adb7
Source noteuspto-grants-1990_09