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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271230Generated: October 25, 2026

Sodium Hydroxide → 4-Bromo-1-indan-5-yloxybutane

https://huagongshe.com/reaction/271230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant5-IndanolHCID 15118—
Reactant2,3-DibromobutaneHCID 21508—
Reactantt-Butylammonium hydrogen sulfateHCID 24996679—
SolventDichloromethaneHCID 6344—
Product4-Bromo-1-indan-5-yloxybutaneHCID 13058965—

Reaction Steps

5-Indanol (1 g, 7.45 mmol) in NaOH(aq) (5.22 mL, 20.88 mmol, 4 M soln.) was treated with dibromobutane (3.38 mL, 28.3 mmol) and t-butylammoniumhydrogensulfate (catalytic). The solution was placed in a Robbins™ oven for 14 hours at 99° C. Upon cooling, the pH was adjusted to ˜8 with 4 N NaOH. CH2Cl2 was then added and the solution washed with H2O (×2) and brine. The organic layer was dried over MgSO4 and concentrated to an oil. The oil was then dissolved in 4:1 hexane/EtOAc and passed through a plug of silica gel which was then washed with 4:1 hexane/EtOAc. The filtrate was concentrated to afford 4-bromo-1-indan-5-yloxybutane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452889B2
Source datasetuspto-grants-2008_11
ORD IDord-8ecafe4ed40148bfb87578ac45b936cd
Source noteuspto-grants-2008_11