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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913402Generated: October 28, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → (R)-1-azido-5-bromo-indane

https://huagongshe.com/reaction/1913402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantDiphenylphosphoryl azideHCID 123414—
Reactant(1S)-5-bromo-2,3-dihydro-1H-inden-1-olHCID 29414737—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product(R)-1-azido-5-bromo-indaneHCID 5917960283.5%

Reaction Conditions

Temperature15 °C

Reaction Steps

A solution of (S)-5-bromo-indan-1-ol (15.0 g, 70.4 mmol) in toluene (150 mL) was cooled in an ice bath under N2 and was treated with diphenylphosphoric azide (DPPA, 22.0 g, 91.5 mmol) in one portion followed by 1,8-diazabicyclo[5,4,0]undec-7-ene (15.0 g, 98.6 mmol). The reaction temperature was kept between 3 and 10° C. during 3 hours of addition and the mixture was warmed to 15° C. over the next hour (TLC indicated no starting material). The mixture was diluted with EtOAc (300 mL) and was washed with water. The organic layer was dried over Na2SO4, filtered and concentrated to give a dark oil. The crude product was purified by silica gel column (packed with 1% Et3N in hexanes, hexane eluant) to give (R)-1-azido-5-bromo-indane (14 g, 83%) as an oil which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609680B2
Source datasetuspto-grants-2013_12
ORD IDord-72eacf37d2454f4ba447640a285f3583
Source noteuspto-grants-2013_12