HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5281Generated: October 26, 2026
1-Octanol → 2-(4-Decyloxyphenyl)-5-octyloxycarbonyl benzooxazole
https://huagongshe.com/reaction/5281
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Octanol | HCID 957 | — |
| Reactant | 4-Pyrrolidinopyridine | HCID 75567 | — |
| Reactant | 2-(4-Decyloxyphenyl)-5-carboxybenzooxazole | HCID 19795409 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Decyloxyphenyl)-5-octyloxycarbonyl benzooxazole | HCID 19795413 | 49.3% |
Reaction Steps
In a 30 ml round-bottom flask, 0.30 g (0.76 m mole) of 2-(4-decyloxyphenyl)-5-carboxybenzooxazole, 0.11 g (0,84 m mole) of octanol and 8 ml of dichloromethane were placed. To the mixture solution 0.16 g (0.78 m mole) of N,N'-dicyclohexycarbodiimide and 0.04 g of 4-pyrrolidinopyridine were added in order under stirring at room temperature, followed by stirring for 8 hours at room temperature to precipitate N,N'-dicyclohexylurea. The resultant N,N'-dicyclohexylurea was filtered off and the filtrate was dried under reduced pressure. The resultant was purified by silica gel column chromatography (eluent: toluene) and recrystallized twice from acetone to obtain 0.19 g of 2-(4-decyloxyphenyl)-5-octyloxycarbonyl benzooxazole (Yield: 49.3%). ##STR89##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05244596 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-2a52736b43a444e09a503ac093ca58e8 |
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| Source note | uspto-grants-1993_09 |
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