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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033849Generated: October 29, 2026

Formic Acid → 2-[(6,11-Dihydro-5H-dibenzo[b,e]azepin-6-yl)methyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1033849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
Reactant2-(5H-Dibenz[b,e]azepin-6-ylmethyl)-1H-isoindole-1,3(2H)-dioneHCID 19024992—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventDimethylformamideHCID 6228—
Product2-[(6,11-Dihydro-5H-dibenzo[b,e]azepin-6-yl)methyl]-1H-isoindole-1,3(2H)-dioneHCID 9946627—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 110.0 kg of 6-phthalimidomethyl-5H-dibenz[b,e]azepine in 911.4 liters of dimethylformamide, 28.7 kg of formic acid and a suspension of 12.5 kg of 10% palladium charcoal in 25 liters of dimethylformamide is fed into a 1200 liter VA-propulsive jet loop reactor. The reaction mixture is heated to 70° C. and hydrogenated under 7 bar of absolute hydrogen pressure. After the catalyst has been filtered off and the reaction equipment and catalyst have been washed with 80 liters of dimethylformamide, 960 liters of dimethylformamide are distilled off from the combined filtrates at 70° to 80° C. After cooling to 50° C., 150 liters of acetone are added, then after further cooling to 15° C. the precipitated crystals are centrifuged off, washed with acetone and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312916
Source datasetuspto-grants-1994_05
ORD IDord-7e6b63768c31432f833c6295e0411a32
Source noteuspto-grants-1994_05