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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433985Generated: October 28, 2026

Ethyl orthoformate → HCID 69666208, compound

https://huagongshe.com/reaction/433985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
ReactantHCID 69666132HCID 69666132—
ProductHCID 69666208HCID 69666208—

Reaction Conditions

Temperature145 °C

Reaction Steps

(2R)-2-[(3-Aminoquinolin-4-yl)amino]butan-1-ol (416.0 g, 1 eq.) and triethylorthoformate (1.2 L, 4 eq.) were combined and slowly heated to 145° C. Ethanol was distilled off as it formed during the reaction. After ˜500 mL of ethanol had been distilled off, the reaction mixture was allowed to cool to 50° C. under a nitrogen atmosphere. Excess triethylorthoformate was removed under reduced pressure to provide crude (2R)-2-(1H-imidazo[4,5-c]quinolin-1-yl)butan-1-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670372B2
Source datasetuspto-grants-2003_12
ORD IDord-82a579cbbc814287b88fc81a16801466
Source noteuspto-grants-2003_12