HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714417Generated: November 2, 2026
Acetic Anhydride → HCID 66693303, compound
https://huagongshe.com/reaction/714417
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | HCID 66692810 | HCID 66692810 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66693303 | HCID 66693303 | — |
Reaction Steps
A suspension of 1-cyclopropyl-3-(1,6-dihydro-6-oxo-1,2-diphenyl-5-pyrimidinyl)-1,3-propanedione (i.e. the product from Example 6, Step A) (165 mg, 0.46 mmol), triethyl orthoformate (0.23 mL, 1.4 mmol), and acetic anhydride (0.92 mL) was heated at 110° C. under a nitrogen atmosphere for 4 h. The residue was dissolved in toluene (5 mL) and the resulting solution was concentrated under reduced pressure at 50° C. The residue was re-dissolved in toluene (5 mL) and the resulting solution was concentrated at 50° C. to give 181 mg of the title compound as a brown oil that was used in the next step without further purification. 1H NMR analysis showed the product to contain a mixture of Z- and E-olefin isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187432B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-5cd37c9029db476598ddfc1c8e2b4efe |
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| Source note | uspto-grants-2015_11 |
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