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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366674Generated: November 3, 2026

Triethyl orthoacetate → HCID 57447045, compound

https://huagongshe.com/reaction/2366674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl orthoacetateHCID 66221—
ReactantHCID 68874499HCID 68874499—
CatalystBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
ProductHCID 57447045HCID 5744704561.5%

Reaction Steps

Ethyl N-(3-aminoquinolin-4-yl)-β-alaninate (9.0 g, 35 mmol) was treated with triethyl orthoacetate (8.91 mL, 48.6 mmol) and pyridinium p-toluenesulfonate (0.200 g) according to the method described in Part A of Example 10 to provide 6.10 g of ethyl 3-(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)propanoate. The reaction was complete in two hours, and a precipitate was removed by filtration from the organic layer during the work-up procedure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697873B2
Source datasetuspto-grants-2014_04
ORD IDord-d8b5139b33604364b8cb825d5e1f42d0
Source noteuspto-grants-2014_04