HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 9863268, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 86758806 | HCID 86758806 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 9863268 | HCID 9863268 | 10% |
Reaction Steps
Thionyl chloride (10 mL) was added with stirring to 12j (200 mg, 0.5 mmol). After 4 h, the reaction mixture was diluted with benzene (50 mL) and evaporated to dryness. The dark orange solid was dissolved in chloroform and ether was added to give a dark orange solid (16 mg, 10%): mp 194-195° C.; IR (neat) 2938, 1665, 1463, 1400, 1292, 1125, 1007, 976 cm−1; 1H NMR (CDCl3, 300 MHz) δ8.67 (d, 1H, J=7.8 Hz), 8.32 (d, 1H, J=8. 0 Hz), 7.68 (t, 1H, J=8.0 Hz), 7.45 (t, 1H, J=7.8 Hz), 7.04 (s, 1H), 4.09 (s, 3H), 4.06 (s, 3H), 3.97 (s, 3H), 3.89 (s, 3H); CIMS m/z (relative intensity) 352 (MH+, 100). Anal. Calcd for C20H17NO5: C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06509344B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-5efd057cd4f64d99898e087883ced9c4 |
| Source note | uspto-grants-2003_01 |