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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328470Generated: October 30, 2026

tert-Butyl isocyanate → HCID 54465920, compound

https://huagongshe.com/reaction/328470

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl isocyanateHCID 62412—
ReactantHCID 152773082HCID 152773082—
ProductHCID 54465920HCID 54465920—

Reaction Steps

5 Parts of methyl 4,4-dimethylallophanimidate and 20 ml of t-butylisocyanate are refluxed overnight. The next day, the solution is evaporated to give an oil, which crystallizes when tirturated with petroleum-ether under cooling. In order to remove some unreacted starting material and byproducts, the solids are first triturated with water and filtered. After drying, the solids are then triturated with carbon tetrachloride and impurities removed by filtration. The carbon tetrachloride filtrate is then evaporated and the residue recrystallized from petroleum-ether to give pure methyl N-dimethylcarbamoyl-4-t-butylallophanimidate (a compound of Formula I), m.p. 96°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04017529
Source datasetuspto-grants-1977_04
ORD IDord-279a6530cc8243d4b65064c41fcad08d
Source noteuspto-grants-1977_04