HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604614Generated: October 27, 2026
Carbon tetrabromide → 5-(Bromomethyl)-6-iodoindane
https://huagongshe.com/reaction/604614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (6-iodo-2,3-dihydro-1H-inden-5-yl)methanol | HCID 57576294 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-(Bromomethyl)-6-iodoindane | HCID 57544355 | — |
Reaction Steps
To a solution of (6-iodo-2,3-dihydro-1H-inden-5-yl)methanol (36 mg, 0.131 mmol) and carbon tetrabromide (52 mg, 0.158 mmol) in CH2Cl2 (1 mL) at 0° C. under N2, was added triphenylphosphine (41 mg, 0.158 mmol). The resulting solution was allowed to warm to room temperature and was stirred for 4 h. Another portion of carbon tetrabromide (52 mg, 0.158 mmol) and triphenylphosphine (41 mg, 0.158 mmol) was added to the mixture at 0° C. The reaction mixture was stirred at room temperature overnight. The reaction mixture was concentrated in vacuo. The residue was purified by flash chromatography (Si, 1% EtOAc in hexanes) to afford 5-(bromomethyl)-6-iodoindane. 1H NMR (500 MHz, CDCl3) δ 7.72 (s, 1H), 7.36 (s, 1H), 4.62 (s, 2H), 2.89 (m, 4H), 2.11-2.07 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07910592B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-aa01116282a241abb930963603823a5c |
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| Source note | uspto-grants-2011_03 |
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