Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866719Generated: October 31, 2026

Acetone → Benzophenone oxime

https://huagongshe.com/reaction/866719

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantTolueneHCID 1140—
Reactant1,1'-[(Chloromethylene)bis(oxy)]dibenzeneHCID 13349935—
ReactantHCID 131711152HCID 131711152—
SolventDiethyl EtherHCID 3283—
ProductBenzophenone oximeHCID 1132476%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101323
Source datasetuspto-grants-1978_07
ORD IDord-9f31bdeaa8e248f6a75cf5d87cba21cc
Source noteuspto-grants-1978_07