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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512073Generated: October 26, 2026

Formaldehyde → Methyl 2-(quinolin-6-yl)acrylate

https://huagongshe.com/reaction/1512073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 6-quinolineacetateHCID 1514202—
Catalyst1-Hexadecanaminium, N,N,N-trimethyl-, sulfate (1:1)HCID 109763—
SolventTolueneHCID 1140—
ProductMethyl 2-(quinolin-6-yl)acrylateHCID 6736857686.3%

Reaction Steps

As shown in step ii of Scheme 1, methyl 2-(quinolin-6-yl)acetate (82 g, 407.5 mmol), paraformaldehyde (25.89 g, 862.1 mmol), K2CO3 (101.4 g, 733.5 mmol), and hexadecyl(trimethyl)ammonium hydrogen sulfate (15.55 g, 40.75 mmol) were taken up in toluene (1.6 liters) and refluxed for 2 hours until the starting material was completely consumed, as monitored by HPLC. The reaction mixture was cooled down using an ice-water bath and filtered through diatomaceous earth. The filtrate was washed with 1 liter of water and the organic layer dried over anhydrous sodium sulfate, filtered, and evaporated under reduced pressure to afford methyl 2-(quinolin-6-yl)acrylate as a clear colorless oil (75.0 g). This material was used immediately without further purification in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217056B2
Source datasetuspto-grants-2012_07
ORD IDord-bb096a718bdb4f8d969d2c257c3b364d
Source noteuspto-grants-2012_07