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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444370Generated: October 30, 2026

Benzene → 3-[5-[1-(4-Chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl]-1-methyl-1-(2,2-dimethoxyethyl)urea

https://huagongshe.com/reaction/444370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
Reactant5-[1-(4-Chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl isocyanateHCID 13020764—
ReactantMethylaminoacetaldehyde dimethylacetateHCID 23463592—
Product3-[5-[1-(4-Chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl]-1-methyl-1-(2,2-dimethoxyethyl)ureaHCID 13020761—

Reaction Steps

At ambient temperatures 3.9 grams (0.033 mole) of methylaminoacetaldehyde dimethylacetate was slowly added to a 30 ml. benzene solution containing 9.2 grams (0.033 mole) of the 5-[1-(4-chlorophenoxy)ethyl]-1,3,4-thiadiazol-2-yl isocyanate dimer (prepared above). The resulting solution was refluxed for 30 minutes to form a yellow solution and then cooled and topped with a roto-vac at 60 degrees centigrade to 12.4 grams of a viscous yellow oil which crystallized upon standing. The entire sample was recrystallized from a minimum amount of ethylacetate/hexane solution. The crystals were filtered off, and dried in a vacuum oven at 80 degrees centigrade to give 8.3 grams of fluffy white crystals of 3-[5-[1-(4-chlorophenoxy)ethyl-]-1,3,4-thiadiazol-2-yl]-1-methyl-1-1(2,2-dimethoxyethyl)urea. Melting point 116-118 degrees centigrade.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04264353
Source datasetuspto-grants-1981_04
ORD IDord-ed33bf100eb34cc08e30d86ba1e63a07
Source noteuspto-grants-1981_04