HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 23519150, compound → HCID 74058493, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 23519150 | HCID 23519150 | — |
| Reactant | (2,2-Dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl chloride | HCID 85435482 | — |
| Product | HCID 74058493 | HCID 74058493 | 49% |
Reaction Steps
Reaction of (2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-acetyl chloride with [N-(3,4-dichlorobenzyl)aminooxy]-acetic acid tert-butyl ester as described in the preparation of compound 1-A gave the title amide as white crystals (49% yield): mp 127-129° C. (ethyl acetate-hexane). 1HNMR 400 MHz (CDCl3) δ (ppm): 1.51 (9H, s, t-Bu), 1.78 (6H, s, CH3), 4.38 (2H, s, CH2), 4.90 (2H, s, CH2), 6.49 (1H, s, CH), 7.28 (1H, dd, J=2.5 Hz and J=8.0 Hz, aromatic), 7.41 (1H, d, J=8.0 Hz, aromatic), 7.53 (1H, d, J=2.5 Hz, aromatic). Anal. calcd for C20H23Cl2NO7: C, 52.19; H, 5.04; N, 3.04. Found: C, 52.25; H, 5.11; N, 2.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06777440B2 |
| Source dataset | uspto-grants-2004_08 |
| ORD ID | ord-225b45208ac147b18c8a0e752581ce24 |
| Source note | uspto-grants-2004_08 |