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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30251Generated: October 30, 2026

Potassium Carbonate → 5,6-Dibromo-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentalene

https://huagongshe.com/reaction/30251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant2-Benzyl-5,6-dibromo-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentaleneHCID 131727030—
SolventMethanolHCID 887—
Solvent1,1-DichloroethaneHCID 6365—
Product5,6-Dibromo-1,2,3,3a,7,7a-hexahydro-4-thia-2-aza-cyclopenta[alpha]pentaleneHCID 59789451—

Reaction Conditions

Temperature22 °C

Reaction Steps

The product from step g) (605 mg, 1.46 mmol) in dichloroethane (7 ml) was treated with powdered K2CO3 (806 mg, 5.84 mmol) and 1-chloroethyl chloroformate (Ace-Cl) (632 μl, 5.84 mmol) at 80° C. for 16 hours. Next, the reaction was cooled, filtered and concentrated providing an oily residue. This oily residue was diluted with anhydrous MeOH (15 ml) and stirred for 1 hour at 22° C. The solvent was concentrated and the crude residue was purified by preparative LC/MS providing title compound. 1H NMR (300 MHz, CD3OD, ppm) 2.65-2.75 (m, 1H); 3.05-3.30 (m, 2H); 3.32-3.80 (m, 4H); 4.10-4.28 (br m, 1H); MS calculated for C9H9Br2NS+H 324, observed 322, 324, 326.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423056B2
Source datasetuspto-grants-2008_09
ORD IDord-b2ba5165d1ec4365a3717803667ac969
Source noteuspto-grants-2008_09