HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(Chloromethyl)benzoyl chloride → HCID 22291052, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(Chloromethyl)benzoyl chloride | HCID 2733324 | — |
| Reactant | HCID 16782558 | HCID 16782558 | — |
| Product | HCID 22291052 | HCID 22291052 | 87% |
Reaction Steps
Using an analogous procedure to that described in Example 2, N-(5-amino-2-methylphenyl)-3,4-dimethoxybenzamide was reacted with 3-(chloromethyl)benzoyl chloride to give the title compound in 87% yield; NMR Spectrum: (DMSOd6) 2.19 (s, 3H), 3.82 (s, 6H), 4.84 (s, 2H), 7.06 (d, 1H), 7.23 (d, 1H), 7.57 (m, 5H), 7.80 (s, 1H), 7.9 (d, 1H), 8.0 (s, 1H), 9.76 (s, 1H), 10.26 (s, 1H); Mass Spectrum: M+H+ 439.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06956037B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-ec5348299f17439eba395b33d1435a1d |
| Source note | uspto-grants-2005_10 |