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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107769Generated: October 30, 2026

18-Crown-6 → HCID 18785577, compound

https://huagongshe.com/reaction/1107769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
Reactant3-Bromo-1,1-dichloroprop-1-eneHCID 12642406—
Reactant7-Benzyloxy-2,3-dimethylpyrrolo[2,3-d]pyridazineHCID 18785683—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18785577HCID 1878557722.6%

Reaction Steps

0.13 g (0.0011 mole) of potassium tert-butoxide was added to a suspension of 0.29 g (0.0011 mole) of 7-benzyloxy-2,3-dimethylpyrrolo[2,3-d]pyridazine and 0.03 g (0.0001 mole) of 18-crown-6 in 8 ml of tetrahydrofuran and the resulting mixture was stirred at room temperature for 40 minutes. 0.22 g (0.0011 mole) of 3,3-dichloro-2-propenyl bromide was then added to the mixture and stirred at room temperature for 5 minutes. The reaction mixture was poured into ice-water and the aqueous mixture was extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by column chromatography through silica gel using a 20:1 mixture of chloroform and methanol as an eluent to give 0.090 g of 7-benzyloxy-1-(3,3-dichloro-2-propenyl)-2,3-dimethylpyrrolo[2,3-d]pyridazine as a yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063782
Source datasetuspto-grants-2000_05
ORD IDord-6a342b8c982a45fe9ba85e96c2e2d926
Source noteuspto-grants-2000_05