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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546325Generated: November 2, 2026

Allyl bromide → HCID 86602875, compound

https://huagongshe.com/reaction/546325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 86602876HCID 86602876—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86602875HCID 86602875—

Reaction Steps

Allyl bromide (52 μL, 0.6 mmol) and DBU (65 μL, 0.6 mmol) were added to a solution of N-ethylcarbamate-5-hydroxy-6-iodo-8-ethyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrrole (116 mg, 0.3 mmol) in CH2Cl2 (3 mL), and stirred 2 hours at room temperature. The reaction solution was diluted with H2O and filtered through an Extrelut column, The column was washed with CH2Cl2 and the filtrate was concentrated. The crude product was purified via silica plug eluting with Hexanes/EtOAc (3/1, v/v) to afford 50 mg (39%-two steps) of the subtitle compound. MS calculated for C18H221NO3+H: 428, observed: 428.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935830B2
Source datasetuspto-grants-2011_05
ORD IDord-0beb956bd60d4bc1aeb85ef773f17218
Source noteuspto-grants-2011_05