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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596729Generated: October 30, 2026

Chloral → HCID 12906108, compound

https://huagongshe.com/reaction/596729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloralHCID 6407—
Reactant(4-Aminophenoxy)benzeneHCID 8764—
ReactantMethyl IsocyanateHCID 12228—
ReactantThionyl ChlorideHCID 24386—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 12906108HCID 1290610820%

Reaction Steps

p-Phenoxyaniline (11.7 g, 0.063 mol) was dissolved in 25 ml. 1,2-dimethoxyethane (Ansul E-121) and heated to 65° C. Methyl isocyanate (3.7 g, 0.65 mol) was added over a period of 10 minutes. Heating and stirring were continued for 1 hour. Then chloral (14.8 g, 0.1 mol) was added to the hot solution, followed immediately by the addition of 11.9 g (0.1 mol) thionyl chloride. It was kept at 65° C. for 41/2 hours. The solution was cooled to 40°, and 25 ml of methylene chloride was added. The solution was refluxed for one more hour and then allowed to cool. The solid which formed upon cooling was filtered, washed with methylene chloride to give 5.0 g (20% yield) of the product, as a white powder, melting point 165°-167° C. A second crop, melting point 160°-162° C., weighed 5.5 g (22%). Elemental analysis showed: %Cl, calc. 34.8, found 34.4; %N, calc. 6.9, found 6.8; %C, calc. 47.1, found 47.5; %H, calc. 3.46, found 3.3. The product is the eighth compound tabulated in Table I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012225
Source datasetuspto-grants-1977_03
ORD IDord-b96ccadb920840f38131dba045c93215
Source noteuspto-grants-1977_03