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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581987Generated: November 1, 2026

Benzyl Bromide → 2-(Tert-butoxycarbonylamino)-5-phenoxyindan

https://huagongshe.com/reaction/1581987

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22719625HCID 22719625—
SolventAcetoneHCID 180—
Product2-(Tert-butoxycarbonylamino)-5-phenoxyindanHCID 2271958690%

Reaction Steps

2-(tert-butoxycarbonylamino)-5-hydroxyindan (100 mg, 0.40 mmol) synthesized in the above Preparation Example 1 was dissolved in acetone (2 ml), to which potassium carbonate (58 mg, 0.45 mmol) and benzylbromide (48 μl, 0.40 mmol) were added, and the mixture was heated to reflux for 3 hours. The reaction mixture was extracted with ether and dried, and then the solvent was distilled off under reduced pressure to obtain 2-(tert-butoxycarbonylamino)-5-phenoxyindan (120 mg, 0.36 mmol) having the following physical properties:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734180B1
Source datasetuspto-grants-2004_05
ORD IDord-fbce2c52d50340f4ad8d6e24d0956d60
Source noteuspto-grants-2004_05