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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377281Generated: October 30, 2026

Hydrochloric Acid → HCID 86755129, compound

https://huagongshe.com/reaction/377281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
Reactant5-Bromoisoindoline hydrobromideHCID 19358359—
SolventDichloromethaneHCID 6344—
ProductHCID 86755129HCID 86755129—

Reaction Steps

In 25 ml of 47% hydrobromic acid was suspended 5.0 g of 5-bromo-2-(p-toluenesulfonyl)isoindoline, followed by adding thereto 4.0 g of phenol and 15 ml of propionic acid, and the resulting mixture was heated under reflux for 4 hours. The reaction mixture was concentrated under reduced pressure, after which ethanol was added to the resulting residue and the crystals were collected by filtration to obtain 3.5 g of 5-bromoisoindoline hydrobromide. The hydrobromide obtained was suspended in 50 ml of methylene chloride, followed by adding thereto 2.8 g of triethylamine. Then, 2.4 g of benzyl chloroformate was added dropwise thereto and the resulting mixture was stirred at room temperature for 1 hour. The reaction mixture was added to 50 ml of water and the pH was adjusted to 1 with 6N hydrochloric acid, after which the organic layer was separated. The organic layer obtained was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. n-Hexane was added to the resulting residue and the crystals were collected by filtration to obtain 3.8 g of colorless 2-benzyloxy-carbonyl-5-bromoisoindoline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06025370
Source datasetuspto-grants-2000_02
ORD IDord-2afab41ecbe7495eaf1cf3e736703faf
Source noteuspto-grants-2000_02