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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862048Generated: October 30, 2026

m-Tolyl isocyanate → HCID 54548162, compound

https://huagongshe.com/reaction/862048

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Tolyl isocyanateHCID 69303—
ReactantHCID 10836729HCID 10836729—
ReactantChloroform methanolHCID 21584188—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54548162HCID 5454816261.6%

Reaction Steps

A mixture of N-benzyloxycarbonyl-(L)-isoleucyl-(L)-tryptophanol (0.7 g) in ethanol (30 ml)-tetrahydrofuran (20 ml), palladium-carbon (5%, 0.5 g) was subjected catalytic hydrogenation at room temperature under 1 atmospheric pressure. After the palladium-carbon was filtered off, the filtrate was concentrated under reduced pressure to yield an oily substance. This oily substance was dissolved in dichloromethane (15 ml)-tetrahydrofuran (5 ml), and m-methylphenyl isocyanate (0.225 g) was added at 4° C. After stirring at room temperature for 1.5 hours, the reaction mixture was poured over chloroform-methanol. After the insoluble substances were filtered off, the filtrate was concentrated under reduced pressure, and the residual solid was recrystallized from dichloromethane-methanol-hexane to yield N-(3-methylphenylcarbamoyl)-(L)-isoleucyl-(L)-tryptophanol (0.43 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716980
Source datasetuspto-grants-1998_02
ORD IDord-e2d42659f98b417395593ad6212a407b
Source noteuspto-grants-1998_02