HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → o-Hydroxyphenyl methylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 13269093 | HCID 13269093 | — |
| Product | o-Hydroxyphenyl methylcarbamate | HCID 82537 | 98% |
Reaction Steps
In fact, the reaction of pyrocatechol carbonate with methylamine in the presence of not less than 1 mol equivalent of the abovementioned secondary amines gives pyrocatechol monomethylcarbamate in a yield of 98-99%. The subsequent reaction of the reaction mixture with 1,2-dichloroethyl methyl ether in turn takes place with a yield of above 90%. Compared with the reaction with tertiary amines, the conversion takes place substantially more rapidly (on the bas-is of experience, from eight to ten times faster) and with better selectivity, and consequently a purer and more stable end product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04788324 |
| Source dataset | uspto-grants-1988_11 |
| ORD ID | ord-f565a8cc4a7b4e75acdcdf4d7a683b3f |
| Source note | uspto-grants-1988_11 |