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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372748Generated: October 25, 2026

1-Methyl-1H-pyrrole-2-carbaldehyde → Methyl (2-(1-methyl-2-pyrrolyl)-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-1H-pyrrole-2-carbaldehydeHCID 14504—
ReactantIodo benzene diacetateHCID 12217721—
ReactantMethyl 2-(4-amino-3-hydroxyphenyl)acetateHCID 17858854—
SolventEthanolHCID 702—
ProductMethyl (2-(1-methyl-2-pyrrolyl)-6-benzoxazolyl)acetateHCID 5877896127.3%

Reaction Steps

In ethanol (10 ml), 1-methylpyrrole-2-carbaldehyde (0.33 ml, 3.09 mmol) and methyl 4-amino-3-hydroxyphenylacetate (559 mg, 3.09 mmol) were stirred for 4 hours at room temperature. Iodobenzene diacetate (1.19 g, 3.70 mmol) was added to the reaction mixture. After stirring at room temperature for 30 minutes, the reaction mixture was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane-ethyl acetate (3:1, v/v) eluate fractions, methyl (2-(1-methyl-2-pyrrolyl)-6-benzoxazolyl)acetate (228 mg, 27%) was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-c5c7f958390d471fab1bd96cf254d830
Source noteuspto-grants-2007_01