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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325254Generated: October 31, 2026

Hexane → HCID 13083045, compound

https://huagongshe.com/reaction/325254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant2-Amino-4-methoxy-6-methyl-1,3,5-triazineHCID 15466—
ReactantHCID 11322793HCID 11322793—
SolventDichloromethaneHCID 6344—
ProductHCID 13083045HCID 1308304589.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04440565
Source datasetuspto-grants-1984_04
ORD IDord-a91458f73cbc4896a6936a8c0c7c8ad7
Source noteuspto-grants-1984_04