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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453532Generated: October 29, 2026

1,3-Dibromopropane → HCID 68624457, compound

https://huagongshe.com/reaction/1453532

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DibromopropaneHCID 8001—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 68624072HCID 68624072—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 68624457HCID 68624457—

Reaction Steps

A solution of (2S)-N-(4-hydroxy-5-methoxy-2-nitrobenzoyl)-4,4-difluoropyrrolidine 2-carboxaldehyde diethylthioacetal IV (1 mmol), 1,3-dibromopropane (0.5 mmol) and K2CO3 (3 mmol) in dry acetone (40 ml) was refluxed for 48 h. After the completion of reaction as indicated by TLC, EtOAc-hexane (6:4), the reaction mixture was poured on to the water and then extracted with ethyl acetate. Evaporation of the organic layer gave the crude product, which was further purified by column chromatography on silica gel eluting with EtOAc-hexane (1:1) to give the pure 1,1′-{[(Propane-1,3diyl)dioxy]bis[2-nitro-5-methoxy-1,4-phenylene)carbonyl]}bis[4,4-difluoropyrrolidine-2-carboxaldehyde diethylthioacetal] V.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476664B2
Source datasetuspto-grants-2009_01
ORD IDord-83895608f6c24f48a2bd63578e25dd9e
Source noteuspto-grants-2009_01