HuagongsheHuagongshe Chemistry Print Report · For research reference only
18-Crown-6 → HCID 13557263, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | HCID 13557273 | HCID 13557273 | — |
| Reactant | HCID 13557277 | HCID 13557277 | — |
| Reactant | Oxazinone | HCID 21873527 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 13557263 | HCID 13557263 | — |
Reaction Steps
This compound was prepared in the manner of Example 1, Step C; using 1.3 grams (0.01 mole) of 5,6-dihydro-4,4-dimethyl-2H-1,2-oxazin-3(4H)-one, 3.1 grams (0.01 mole) of 2-chloro-4-[(N-methoxy-N-methylamino)carbonylamino]phenylmethyl bromide, 1.4 grams (0.01 mole) of potassium bromide and 0.1 gram (0.0004 mole) of 1,4,7,10,13,16-hexaoxacyclooctadecane in 50 ml of acetonitrile. The yield of 2-(2-chloro-4-[(N-methoxy-N-methylamino)carbonylamino]phenyl)methyl-5,6-dihydro-4,4-dimethyl-1H-1,2,-oxazin-3(4H)-one was 2.9 grams; m.p. 116°-118° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04552585 |
| Source dataset | uspto-grants-1985_11 |
| ORD ID | ord-b9d674cfcba04477adfa1d8a852f20f5 |
| Source note | uspto-grants-1985_11 |