HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382918Generated: November 1, 2026
Triphenylphosphine → HCID 21273347, compound
https://huagongshe.com/reaction/1382918
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 13983022 | HCID 13983022 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 21273347 | HCID 21273347 | 35.4% |
Reaction Steps
A mixture of 7.25 g (28.4 mmole) of 6-bromomethyl-4,4-dimethylchroman, 14.8 g (56.8 mmole) of triphenylphosphine and 100 ml of toluene were heated under reflux for 12 hours, and then the solvent was removed by evaporation in vacuo. The residue (an oil) was dissolved in dichloromethane and decolorized with activated carbon. The solvent was removed by evaporation in vacuo and the residue was triturated under hexane to remove starting materials. The product so obtained was recrystallized from toluene-chloroform and the solid was discarded. The recrystallization mother liquors were evaporated in vacuo and the oily residue was triturated under 1N hydrochloric acid and then dissolved in dichloromethane. This latter solution was dried (MgSO4) and evaporated in vacuo to give 5.2 g of the title compound as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04808597 |
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| Source dataset | uspto-grants-1989_02 |
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| ORD ID | ord-283b7b7813694d2daa51ed6208304d04 |
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| Source note | uspto-grants-1989_02 |
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