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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975138Generated: October 29, 2026

Sodium Iodide → HCID 22859588, compound

https://huagongshe.com/reaction/975138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
ReactantBromomethylcyclopropaneHCID 81503—
Reactant1H-Indole, 5-bromo-3-(2-pyrrolidinylmethyl)-, (R)-HCID 22859590—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 22859588HCID 2285958899.5%

Reaction Steps

A stirred mixture of 5-bromo-3-(2(R)-pyrrolidinylmethyl)-1H-indole (Preparation 2; 1.84 g, 6.3 mmol), cyclopropylmethyl bromide (0.67 ml, 6.9 mmol), anhydrous sodium carbonate (0.73 g, 6.9 mmol), sodium iodide (1.0 g, 6.7 mmol) and 1,2-dimethoxyethane (10 ml), under nitrogen, was heated under reflux for 14 hours, allowed to cool, then partitioned between ethyl acetate and 2M aqueous sodium carbonate solution. The organic phase was separated, washed with 2M aqueous sodium carbonate solution, dried (Na2SO4) and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with 0.880 aqueous ammonia:methanol: dichloromethane (0.05:10:90), to provide the required product as a foam (2.09 g). Rf 0.24 (SS 6). [α]D25 +72° (c=0.1, CH3OH). Found: C,61.22; H,6.40; N,8.39. C17H21BrN2 requires C,61.26; H,6.35; N,8.41%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607960
Source datasetuspto-grants-1997_03
ORD IDord-0ec2ca87d71e4dd0ab754d8ff3a8c627
Source noteuspto-grants-1997_03