HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255546Generated: November 1, 2026
Trifluoroacetic acid → HCID 131718100, compound
https://huagongshe.com/reaction/2255546
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | HCID 131718101 | HCID 131718101 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131718100 | HCID 131718100 | — |
Reaction Steps
A solution of 2-n-butyl-3-[(2'-(t-butoxycarbonyl)biphen-4-yl)-methyl]-6-isopropylquinazolin-4(3H)-one (0.198 g, 0.44 mmol) from Example 36B in a mixture of methylene chloride (3 ml) and anhydrous trifluoro acetic acid (3 ml) containing anisole (0.05 ml) was stirred at room temperature for 4 hours. The solvent was then removed under reduced pressure and the residue was triturated with dry ether to give the solid product, which was then collected by filteration and dried in vacuo over NaOH and P2O5 to give the desired product as the mono trifluoroacetate salt. 1H-NMR(CDCl3): 0.91 (t, 3H, J=7.35 Hz), 1.32 (d, 6H, J=6.9 Hz), 1.47 (m, 2H), 1.72 (m, 2H), 3.12 (m, 3H), 5.48 (s, 2H), 7.14-7.96 (m, 11H), 8.16 (d, 1H, J=1.9 Hz). FAB-MS: m/e 399 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05240928 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-bf4a2846329d494dbdc06ea03f7764b7 |
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| Source note | uspto-grants-1993_08 |
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