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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357719Generated: October 25, 2026

Indene → (1R,2R)-2-bromo-2,3-dihydro-1H-inden-1-ol

https://huagongshe.com/reaction/357719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndeneHCID 7219—
ReactantX 100HCID 19153—
ReactantBromineHCID 24408—
SolventWaterHCID 962—
Product(1R,2R)-2-bromo-2,3-dihydro-1H-inden-1-olHCID 820607—

Reaction Steps

43.5 g of indene (92 wt %; 0.345 mol), 0.7 g of Triton X-100 and 100 ml of water were put into a 500-ml 3-mouthed flask, and mixed by stirring. Mixing was continued at 60° C. as 27.5 g of bromine (0.172 mol, 0.5 mol/mol of indene) was added dropwise over approximately 3 hours. After this, stirring at 60° C. was continued. The reaction mixture was extracted with ethyl acetate directly after dropwise addition of bromine, and after mixing for a further 1 hour. Yields of trans-2-bromoindan-1-ol were calculated from the hydrogen bromide concentrations in the aqueous phase (by gravimetric titration using silver nitrate), and the quantity of indene in the extraction layer was found by GC by means of a calibration line and used to calculate percent conversion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05841000
Source datasetuspto-grants-1998_11
ORD IDord-5e3b608a02844ee681a9b9028f921b75
Source noteuspto-grants-1998_11