HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561841Generated: October 26, 2026
Tributylphosphine → 2-(3-(4-Bromophenyl)propoxy)-3-chloro-1,4-difluorobenzene
https://huagongshe.com/reaction/561841
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | 2-Chloro-3,6-difluorophenol | HCID 2773561 | — |
| Reactant | 3-(4-Bromophenyl)propan-1-ol | HCID 10560614 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(3-(4-Bromophenyl)propoxy)-3-chloro-1,4-difluorobenzene | HCID 66760972 | — |
Reaction Steps
3-(4-Bromophenyl)propan-1-ol from the previous step (1 eq.) and 2-chloro-3,6-difluorophenol (1 eq.) were taken up in freshly deoxygenated toluene (0.3 M). To this solution was then added 1,1′-(azodicarbonyl)-dipiperidine (1.2 eq.) and finally tributylphosphine (1.2 eq.). The resulting yellow solution was heated at 80° C. for 2 h. The reaction mixture was cooled to RT, diluted with ether, and washed with 1 N aq. NaOH. The aqueous wash was back extracted with ether and the combined organic extracts were dried over MgSO4. Filtration and concentration of the filtrate in vacuo afforded a yellow semi-solid. Purification of the crude product thus obtained by way of flash chromatography (SiO2, Hex→15:1 (v/v) Hex:EtOAc) afforded the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063105B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-3113e977140649649adde3ee3d4a5b46 |
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| Source note | uspto-grants-2011_11 |
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