HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862048Generated: October 30, 2026
m-Tolyl isocyanate → HCID 54548162, compound
https://huagongshe.com/reaction/862048
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Tolyl isocyanate | HCID 69303 | — |
| Reactant | HCID 10836729 | HCID 10836729 | — |
| Reactant | Chloroform methanol | HCID 21584188 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54548162 | HCID 54548162 | 61.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05716980 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-e2d42659f98b417395593ad6212a407b |
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| Source note | uspto-grants-1998_02 |
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