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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706135Generated: November 1, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 20337305, compound

https://huagongshe.com/reaction/1706135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantSKF-38393 (hydrobromide)HCID 12928470—
SolventMethanolHCID 887—
ProductHCID 20337305HCID 2033730597%

Reaction Steps

To a suspension of 7,8-dihydroxy-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrobromide (34 g, 0.101 mole, U.S. Pat. No. 3,393,192) in methanol (275 ml) was added a solution of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (25.2 g, 0.111 mole) in methanol (125 ml). The addition was carried out rapidly with stirring at 0° under an argon atmosphere. After stirring at 0° for 1 hour the reaction mixture was filtered and the orange precipitate was washed with cold methanol (75 ml), ethyl acetate (100 ml) and then diethyl ether (100 ml). After drying at room temperature under vacuum, 1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-dione hydrobromide (32.8 g, 0.98 mole, 97%) was obtained, mp 164°-165° (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04206210
Source datasetuspto-grants-1980_06
ORD IDord-fc4ea691aef94857966275080c3aa70e
Source noteuspto-grants-1980_06