HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 13340644, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13340643 | HCID 13340643 | — |
| Product | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 13340644 | HCID 13340644 | 52% |
Reaction Steps
To a suspension of 8.3 g (0.02 m) of 4,10-dihydro-N-(1-hydroxy-2-methyl-2-propyl)-10-oxothieno[3,2-c][1]benzoxepin-8-yl acetamide of Example 1 and 200 ml of methylene chloride, SOCl2 (3.09 g) was added dropwise keeping the temperature at approximately 5° C. The suspended material gradually dissolved. The mixture was stirred overnight (about 16 hours). The organic layer was washed with 10% NaOH, dried (Na2SO4) and evaporated to give an oil. Trituration with isopropyl ether gave 4.1 g (52%) of 2-(4,10-dihydro-10-oxothieno[3,2-c][1]benzoxepin-8-yl)methyl-4,4-dimethyl-oxazoline, m.p. 85°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04514411 |
| Source dataset | uspto-grants-1985_04 |
| ORD ID | ord-b260a6e6248b41cba33d4efe729939a3 |
| Source note | uspto-grants-1985_04 |