HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653813Generated: October 28, 2026
Phosphorus oxychloride → HCID 20080541, compound
https://huagongshe.com/reaction/1653813
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 20080527 | HCID 20080527 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20080541 | HCID 20080541 | 87% |
Reaction Steps
4,5-Bis(4-chlorophenyl)-2-(5-bromopentyl)oxazole is prepared in the following manner: 39.5 g of 1,2-bis(4-chlorophenyl)-2-(6-bromohexanamido)ethanone in 80 cm3 of toluene containing 40 g of phosphorus oxychloride are stirred for 3 hours at 80° C. After evaporation to dryness under vacuum, 100 cm3 of ice-cold water are added. The mixture is extracted with diethyl ether (3 times 120 cm3) and the ethereal solutions are washed successively with water (3 times 50 cm3) and saturated aqueous sodium bicarbonate solution (twice 100 cm3). The organic phase is dried and concentrated to dryness. The solid residue is dissolved in 400 cm3 of hexane, the solution is treated with animal charcoal and filtered through kieselguhr, the filtrate is cooled to 10° C. and the precipate is drained and dried. 33 g (87%) of 4,5-bis(4-chlorophenyl)-2-(5-bromopentyl)oxazole are obtained in the form of white crystals, melting point 98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403852 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-7603c160e3b64f0781b0f718406a87d4 |
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| Source note | uspto-grants-1995_04 |
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