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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44256Generated: October 25, 2026

Methane, dichloromethoxy- → 5-Trichloroacetyl-1H-pyrrole-3-carbaldehyde

https://huagongshe.com/reaction/44256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethane, dichloromethoxy-HCID 21004—
Reactant2-(Trichloroacetyl)pyrroleHCID 321487—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethane nitromethaneHCID 23431834—
Product5-Trichloroacetyl-1H-pyrrole-3-carbaldehydeHCID 12459977—

Reaction Steps

To a solution of the compound obtained in Step A (87 mmoles) and AlCl3 in a DCM/nitromethane mixture (80 ml/80 ml) there is added, dropwise, at −30° C., dichloro-methoxy-methane (130.5 mmoles). After stirring for two hours, the reaction mixture is poured into 800 ml of ice-cold water. The aqueous phase is extracted with AcOEt, and then the organic phases are combined. The organic phase is washed with saturated aqueous NaCl solution, dried over sodium sulphate, filtered and evaporated to dryness to yield the title product (brown crystals), which is used directly in the next Step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541412B2
Source datasetuspto-grants-2013_09
ORD IDord-00e8b7f346ed4dddbda4d8e0c9474695
Source noteuspto-grants-2013_09