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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409980Generated: October 25, 2026

5-(Chloromethyl)-1,2,3-trimethoxybenzene → Ethyl 1-(3,4,5-trimethoxybenzyl)-3-(trimethylsilyl)-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1409980

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Chloromethyl)-1,2,3-trimethoxybenzeneHCID 77448—
ReactantEthyl 1-(2-(2,5-dimethoxyphenyl)-2-oxoethyl)-3-(pyridin-3-yl)-1H-pyrazole-5-carboxylateHCID 86267540—
ReactantEthyl 3-(trimethylsilyl)-1H-pyrazole-5-carboxylateHCID 178469409—
ProductEthyl 1-(3,4,5-trimethoxybenzyl)-3-(trimethylsilyl)-1H-pyrazole-5-carboxylateHCID 86267743—

Reaction Steps

This compound was made in an analogous fashion to ethyl 1-(2-(2,5-dimethoxyphenyl)-2-oxoethyl)-3-(pyridin-3-yl)-1H-pyrazole-5-carboxylate using ethyl 3-(trimethylsilyl)-1H-pyrazole-5-carboxylate and 3,4,5-trimethoxy benzyl chloride (purchased from Aldrich). 1H-NMR δ 6.98 (s, 1H), 6.21 (s, 2H), 5.44 (s, 2H), 4.41 (q, 2H), 3.81 (s, 3H), 3.76 (s, 6H), 1.40 (t, 3H), 0.22 (s, 9). Calculated mass for C19H28N2O5Si, 392.18, observed, 393.0 (M+1), 415.1 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921401B2
Source datasetuspto-grants-2014_12
ORD IDord-8ae9ffc3117742dfa22ce29c5930932f
Source noteuspto-grants-2014_12