HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Benzophenone oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1,1'-[(Chloromethylene)bis(oxy)]dibenzene | HCID 13349935 | — |
| Reactant | HCID 131711152 | HCID 131711152 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzophenone oxime | HCID 11324 | 76% |
Reaction Steps
are reacted in each case with 5 g of diphenoxy chloromethane. By a thin-layer chromatographic process (silica gel plates, 9:1 mixture of toluene and acetone as the eluant), practically uniform, oily crude products are obtained, viz. the following diphenoxy-methyloxime ethers: (a) Compound No. 86 (yield: 77% of theoretical), (b) Compound No. 87 (yield: 92% of theoretical), (c) Compound No. 88 (yield: 86% of theoretical), and d) the o-diphenoxy-methyl-benzophenone-oxime designated as Compound No. 89 (yield: 76% of theoretical) which is obtained by recrystallization of the crude product from ether and has a melting point of 89°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101323 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-9f31bdeaa8e248f6a75cf5d87cba21cc |
| Source note | uspto-grants-1978_07 |