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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296374Generated: October 31, 2026

HCID 12070472, compound → HCID 12070473, compound

https://huagongshe.com/reaction/1296374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 12070472HCID 12070472—
ReactantHCID 178418361HCID 178418361—
ProductHCID 12070473HCID 1207047370%

Reaction Steps

An autoclave was charged, 10 mmole of 1-acetyloxy-3-nitroadamantane obtained by the method of Example 14, 5% Pd-C (10 mole % of Pd relative to a substrate), 1 ml of dilute hydrochloric acid and 10 ml of methanol. The mixture was stirred for 2 hours at 80° C. in an atmosphere of hydrogen at 30 atm. As a result, the conversion of 1-acetyloxy-3-nitroadamantane was 90%, and 1-acetyloxy-3-aminoadamantane (yield 70%) was formed.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039744E1
Source datasetuspto-grants-2007_07
ORD IDord-62462b1dea9a4ff0814ac900a768d06f
Source noteuspto-grants-2007_07