HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(2,4-Difluorobenzyloxy)-5-formylbenzoic acid → n,n-Di-n-pentyl-2-(2,4-difluorobenzyloxy)-5-formylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(2,4-Difluorobenzyloxy)-5-formylbenzoic acid | HCID 22716808 | — |
| Reactant | n,n-Di-n-pentyl-2-methoxy-5-formylbenzamide | HCID 22716819 | — |
| Product | n,n-Di-n-pentyl-2-(2,4-difluorobenzyloxy)-5-formylbenzamide | HCID 11258993 | — |
Reaction Steps
N,N-Di-n-pentyl-2-(2,4-difluorobenzyloxy)-5-formylbenzamide was prepared from 2-(2,4-difluorobenzyloxy)-5-formylbenzoic acid (200 mg, 1 eq) using the same procedure as for N,N-di-n-pentyl-2-methoxy-5-formylbenzamide. The product was obtained as a pale brown oil (442 mg, 99%). 1H NMR (CDCl3) δ9.89 (s, 1H, O═C—H), 5.22 (d, 1H, CH2Ar), 5.10 (d, 1H, CH2Ar), 3.74 (m, 1H, NCH2), 3.14 (m, 1H, NCH2), 3.05 (m, 2H, NCH2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06740670B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-41fa2da194c545d78f11b6e8a2b0e592 |
| Source note | uspto-grants-2004_05 |