HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dichloroacetone → 4-(Chloromethyl)-2-(3,4-dihydronaphthalen-2-yl)oxazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | 3,4-Dihydro-2-naphthalenecarboxamide | HCID 22009819 | — |
| Product | 4-(Chloromethyl)-2-(3,4-dihydronaphthalen-2-yl)oxazole | HCID 22009637 | 60% |
Reaction Steps
In substantially the same manner as in Reference Example 31, 3,4-dihydro-2-naphthalenecarboxamide was allowed to react with 1,3-dichloroacetone to give 4-chloromethyl-2-(3,4-dihydro-2-naphthyl)oxazole. The yield was 60%. Recrystallization from isopropyl ether gave colorless prisms, mp 73-74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06211215B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-925a11c0d6e349ac82ecc515deccfd8e |
| Source note | uspto-grants-2001_04 |