HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 334017, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 23663841 | HCID 23663841 | — |
| Product | HCID 334017 | HCID 334017 | — |
Reaction Steps
(R/S)-N-Benzoyl-2-(4'-methoxyphenyl)-1,3-oxazolidin-5-one (21) was prepared from sodium N-(para-methoxybenzylidene)-glycinate (2.15 g, 10.0 mM) and benzoyl chloride (1.16 mL, 10.0 mM) following general procedure D and obtained as a white solid after purification by flash column chromatography, using 20% ethyl acetate/petrol as eluant (2.08 g, 70%): mp 130-132° C.; IR (KBr): 1795, 1635 cm-1 ; 1H NMR (200 MHz, CDCl3): δ 6.84-7.55 (m, 10H), 4.35 (br, 2H), 3.78 (s, 3H); 13C NMR (50.3 MHz, CDCl3): 169.4, 169.3, 160.6, 133.6, 131.6, 128.6, 128.3, 127.7, 127.5, 114.3, 89.9, 55.4, 46.7; LRMS (EI): 298 (MH+). Anal. Calcd for C17H15NO4 : C, 68.68; H, 5.05; N, 4.71; found: C, 68.62; H, 5.01; N, 4.57.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06043278 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-4ea0634532bd470eaf10ea8ffb8211b0 |
| Source note | uspto-grants-2000_03 |