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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indene | HCID 7219 | — |
| Reactant | X 100 | HCID 19153 | — |
| Reactant | Bromine | HCID 24408 | — |
| Solvent | Water | HCID 962 | — |
| Product | (1R,2R)-2-bromo-2,3-dihydro-1H-inden-1-ol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05841000 |
|---|
| Source dataset | uspto-grants-1998_11 |
|---|
| ORD ID | ord-5e3b608a02844ee681a9b9028f921b75 |
|---|
| Source note | uspto-grants-1998_11 |
|---|