HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → N-[(2-Adamantyloxy)carbonyl]-alpha-trimethylsilylethoxymethyl-DL-tryptophan methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-adamantyl Chloroformate | HCID 10878537 | — |
| Reactant | alpha-trimethylsilylethoxymethyl-DL-tryptophan methyl ester | HCID 86747504 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[(2-Adamantyloxy)carbonyl]-alpha-trimethylsilylethoxymethyl-DL-tryptophan methyl ester | HCID 86747503 | 67.8% |
Reaction Steps
A mixture of α-trimethylsilylethoxymethyl-DL-tryptophan methyl ester (1.0 g, 2.8 mmol), diisopropylethylamine (0.4 g, 3 mmol) and 2-adamantylchloroformate (0.65 g, 3 mmol) in 20 mL dry THF was stirred at room temperature for 4 hours. The reaction mixture was diluted with distilled water and extracted with ethyl acetate (4×50 mL). The organic extract was washed with brine and dried over Na2SO4. Evaporation of the organic solvent gave the title compound as a colorless foam (1.0 g, 67.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05278316 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-24b8e15fc3534551a8a29f6197cc7fe9 |
| Source note | uspto-grants-1994_01 |