HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816403Generated: October 31, 2026
HCID 22493731, compound → HCID 22493724, compound
https://huagongshe.com/reaction/1816403
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22493731 | HCID 22493731 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22493724 | HCID 22493724 | 87.5% |
Reaction Steps
A red mixture of acetone O-[5-methoxy-2-(4-methoxy-2,5-dipropylbenzoyl)phenyl]oxime (2.30 g, 5.79 mmol) in acetonitrile (43 mL) and 5% aqueous HCl (32 mL) was stirred at 80° C. for 4 h. Most of the acetonitrile was removed in vacuo and extraction was conducted in CH2Cl2 (3×60 mL) with 33% saturated brine (50 mL). Flash chromatography with silica gel (gradient to 8% EtOAc/hexanes) provided the title compound as a colorless oil (1.72 g, 87% yield for two steps): 1H NMR (300 MHz, CDCl3) δ 0.84 (t, 3H, J=7.3 Hz), 0.96 (t, 3H, J=7.4 Hz), 1.58 (m, 4H), 2.60 (t, 2H, J=7.6 Hz), 2.70 (t, 2H, J=7.8 Hz), 3.89 (s, 3H), 3.92 (s, 3H), 6.84 (s, 1H), 6.92 (dd, 1H, J=8.7, 2.1 Hz), 7.05 (d, 1H, J=2.0 Hz), 7.23 (s, 1H), 7.40 (d, 1H, J=8.7 Hz); MS m/e 340 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884814B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-6e0071b374244f70a1b53d2e2eadf09d |
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| Source note | uspto-grants-2005_04 |
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