Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615420Generated: October 29, 2026

3-Aminophenol → HCID 20428218, compound

https://huagongshe.com/reaction/615420

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminophenolHCID 11568—
Reactant4-AminothiophenolHCID 14510—
ReactantHCID 20428219HCID 20428219—
ReactantHCID 20836576HCID 20836576—
SolventDiethyl EtherHCID 3283—
ProductHCID 20428218HCID 20428218—

Reaction Steps

The process of Example XIX was again practiced except that 59.95 parts of m-aminophenol was substituted for the p-aminothiophenol and 78.9 parts of Bis-(chloropropyl)tetramethyldisiloxane was substituted for the Bis-(chlorobutyl)tetramethyldisiloxane, and the phase transfer catalyst was 3 grams of 18 crown -6 ether. The end product was recovered at a temperature within the range of from 245° C. to 260° C. at from 0.5 mm to 2.0 mm of mercury. The recovered product was identified as Bis-(m-aminophenoxypropyl)tetramethyldisiloxane. The recovered product material was a pale yellow liquid which did not solidify upon standing in the cold at 0° C. for 3 days. Its purity, as determined by titration with perchloric acid, was better than 99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04499149
Source datasetuspto-grants-1985_02
ORD IDord-593adb76224a44c78b7ebd115de46b70
Source noteuspto-grants-1985_02