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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111473Generated: October 30, 2026

HCID 19753326, compound → HCID 178443240, compound

https://huagongshe.com/reaction/1111473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19753326HCID 19753326—
ReactantHCID 178443242HCID 178443242—
ReactantHCID 178516607HCID 178516607—
ProductHCID 178443240HCID 178443240—

Reaction Steps

The yield relative to 2-hydroxy-1,4-naphthoquinone used for the preparation of 2-(1 butylaminododecyl)-3-hydroxy-1,4-naphthoquinone, was 80.1 mol%. Further, the yield relative to the starting material 2-(1-butylaminododecyl)-1,4-naphthoquinone, was 81.7 mmol%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04980489
Source datasetuspto-grants-1990_12
ORD IDord-9eda663651484dd09a500fd1dd4683e1
Source noteuspto-grants-1990_12