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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419095Generated: November 2, 2026

Cyclobutanone → HCID 20316893, compound

https://huagongshe.com/reaction/2419095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanoneHCID 14496—
ReactantHCID 12353616HCID 12353616—
ProductHCID 20316893HCID 20316893—
ProductHCID 20316906HCID 20316906—

Reaction Steps

In a manner similar to that of Example 23, 1 part of 2-amino-5,6-dihydroxy-3,4-dihydro-1(2H)-naphthalenone hydrobromide is reacted with 20 volume parts of cyclobutanone. Via 2-cyclobutylideneamino-5,6-dihydroxy-3,4-dihydro-1(2H)-naphthalenone, 0.5 part of 2-cyclobutylamino-1,5,6-trihydroxy-1,2,3,4-tetrahydronaphthalene hydrobromide is obtained as colorless crystals melting at 190°-200° C (decomposition). This product was identified as the compound according to Example 35 by mixed melting point.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04104402
Source datasetuspto-grants-1978_08
ORD IDord-2adc1c5c2af148c19ac9d60e97f9163a
Source noteuspto-grants-1978_08