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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625397Generated: October 31, 2026

Trityl chloride → 5-Bromo-2-trityl-isoindoline

https://huagongshe.com/reaction/1625397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
Reactant5-BromoisoindolineHCID 14795871—
SolventDichloromethaneHCID 6344—
Product5-Bromo-2-trityl-isoindolineHCID 5926311385.5%

Reaction Steps

Trityl chloride (2.30 g, 8.23 mmol) was added to a solution of 5-bromo-2,3-dihydro-1H-isoindole (1.64 g, 8.23 mmol) and triethylamine (1.4 mL, 9.9 mmol) in dichloromethane (20 mL). After 18 hours the solvent was removed in vacuo, the residue taken up in ethyl acetate and washed with water (×2) and brine, dried (MgSO4) and concentrated. The crude material was purified by flash chromatography on silica eluting with 1% triethylamine/10% ethyl acetate/petrol to give 5-bromo-2-trityl-2,3-dihydro-1H-isoindole as a reddish-brown solid (3.10 g, 85%). 1H NMR (CDCl3) 7.91-7.84 (1H, m), 7.57 (6H, d), 7.45-7.41 (1H, m), 7.33-7.14 (9H, m), 6.95 (1H, d), 3.90 (2H, s), 3.86 (2H, s). MS: Ph3C+ 243.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779132B2
Source datasetuspto-grants-2014_07
ORD IDord-b5e8f53eff524ab28f37652923f022c6
Source noteuspto-grants-2014_07