HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → HCID 13083045, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2-Amino-4-methoxy-6-methyl-1,3,5-triazine | HCID 15466 | — |
| Reactant | HCID 11322793 | HCID 11322793 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13083045 | HCID 13083045 | 89.5% |
Reaction Steps
14.0 g (0.1 mole) of 2-amino-4-methoxy-6-methyl-1,3,5-triazine were suspended in 250 ml of dichloromethane, and a solution of 25.5 g (0.1 mole) of 2,2,2-trichloro-eth-1-oxysulfonyl isocyanate in 100 ml of dichloromethane was added dropwise at 0° to 5° C. The reaction mixture was further stirred for 18 hours at room temperature and cooled to 0° C., and n-hexane was added. The precipitated reaction product was filtered off under suction and recrystallized from absolute ethanol. 35.3 g (89.4% of theory) of N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-N'-(2,2,2-trichloro-eth-1-oxy-sulfonyl)-urea of melting point 128° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04440565 |
| Source dataset | uspto-grants-1984_04 |
| ORD ID | ord-a91458f73cbc4896a6936a8c0c7c8ad7 |
| Source note | uspto-grants-1984_04 |