Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | N-benzyloxycarbonyl-l-tyrosine | HCID 712438 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13210175 | HCID 13210175 | — |
Reaction Steps
1.04 Grams of Z-Tyr-OH was dissolved in 30 ml of tetrahydrofuran, to this solution 0.38 g of N-hydroxysuccinimide was added, then the reaction mixture was ice-cooled, 0.68 g of dicyclohexylcarbodiimide was added under ice-cooled condition, and the whole mixture was stirred at 4° C. for 18 hours. The precipitate formed was removed by suction filtration, the filtrate was subjected to distillation under a reduced pressure, to the residue obtained was added ethyl ether and petroleum ether and was decanted, then dried to obtain the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04474754 |
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| Source dataset | uspto-grants-1984_10 |
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| ORD ID | ord-fbe6ac0f3c7e45c78b5bbebe1b33b03f |
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| Source note | uspto-grants-1984_10 |
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