HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1-[4-(2,3-Dihydro-2,2-dimethyl-6-benzofuranylmethyloxy)phenyl]-3-methoxy-3-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-methoxy-N-methylcarbamoyl chloride | HCID 2734926 | — |
| Reactant | 4-(2,3-Dihydro-2,2-dimethyl-6-benzofuranylmethyloxy)aniline | HCID 22164533 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-[4-(2,3-Dihydro-2,2-dimethyl-6-benzofuranylmethyloxy)phenyl]-3-methoxy-3-methylurea | HCID 14499869 | 65.7% |
Reaction Steps
6.9 g of 4-(2,3-dihydro-2,2-dimethyl-6-benzofuranylmethyloxy)aniline was dissolved into 70 ml of N,N-dimethylformamide, and 2.8 g of triethylamine was added thereto. 3.8 g of N-methoxy-N-methylcarbamoyl chloride was slowly added dropwise thereto. After the mixture was stirred at room temperature, the reaction mixture was poured into water and extracted with ethyl acetate. After the organic layer was washed with water, it was dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off and the residue was subjected to silica gel column chromatography using ethyl acetate/n-hexane (1/2) as a developer to obtain 6.0 g of Compound No. 4 shown in Table 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04959092 |
| Source dataset | uspto-grants-1990_09 |
| ORD ID | ord-61e3415f67074570a9d5168039f43998 |
| Source note | uspto-grants-1990_09 |