HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Isocyanato-2,2,4,4-tetrefluoro-1,3-benzodioxene → HCID 59252134, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Isocyanato-2,2,4,4-tetrefluoro-1,3-benzodioxene | HCID 2775207 | — |
| Reactant | HCID 60125954 | HCID 60125954 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59252134 | HCID 59252134 | — |
Reaction Steps
To a stirring solution of 2,2,4,4-tetrafluoro-6-isocyanato-1,3-benzodioxene (0.816 g, 3.28 mmol) was added 4-(3-aminophenoxy)pyridine-2-carboxylic acid methyl ester (0.800 g, 3.28 mmol) in DCM (13 mL) in portions. The homogenous contents turned white and opaque within 1 min. of addition, and were allowed to stir at room temperature for 12 h. The heterogenous mixture was filtered, and solid product repeatedly washed with DCM to remove residual starting material. The desired product was collected as a white powder, 1.36 g (83%). 1H-NMR (DMSO-d6) δ 9.08 (d, 2H), 8.59 (s, 1H), 8.07 (s, 1H), 7.60 (dd, 1H), 7.37 (m, 4H), 7.25 (d, 1H), 7.20 (dd, 1H), 6.80 (d, 1H), 3.82 (s, 3H); MS LC MS [M+H]+=494.1, RT=3.23 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08076488B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-e9a50958289a44729aba07b748ec6cc4 |
| Source note | uspto-grants-2011_12 |