HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306764Generated: October 31, 2026
Carbon tetrabromide → HCID 22610214, compound
https://huagongshe.com/reaction/2306764
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22610231 | HCID 22610231 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22610214 | HCID 22610214 | — |
Reaction Steps
4.9 g of carbon tetrabromide were dissolved in 75 ml of methylene chloride and treated dropwise with a solution of 7.7 g of triphenylphosphine in 80 ml of methylene chloride at a temperature of −20° C. The slightly orange solution was stirred at 0° C. for 15 minutes, then treated with a solution of 2 g of 4,4,7,7-tetramethyl-2-pentyl-2,3,4,5,6,7-hexahydro-1H-indene-2-carbaldehyde in 20 ml of methylene chloride. the reaction mixture was stirred at room temperature for 2 hours, then poured on ice/water and diluted aqueous sodium bicarbonate solution and extracted with methylene chloride. The yellow oil which was received after drying of the organic phase and evaporation of the solvent, was further purified with flash chromatography (silica gel, hexane/ethyl acetate=20:1) to give 2-(2,2-dibromo-vinyl)-4,4,7,7-tetramethyl-2-pentyl-2,3,4,5,6,7-hexahydro-1H-indene as a slightly yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06828337B2 |
|---|
| Source dataset | uspto-grants-2004_12 |
|---|
| ORD ID | ord-52eeef5c144b4872b429cce8ab540f6f |
|---|
| Source note | uspto-grants-2004_12 |
|---|