HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl isocyanate → HCID 54465920, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl isocyanate | HCID 62412 | — |
| Reactant | HCID 152773082 | HCID 152773082 | — |
| Product | HCID 54465920 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04017529 |
| Source dataset | uspto-grants-1977_04 |
| ORD ID | ord-279a6530cc8243d4b65064c41fcad08d |
| Source note | uspto-grants-1977_04 |