Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyethanol | HCID 8019 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 15330044 | HCID 15330044 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22276584 | HCID 22276584 | 62.9% |
Reaction Steps
To a solution of N-(t-butoxycarbonylaminosulfonyloxy)-succinimide (272 mg), 2-methoxyethanol (84.4 mg) and triphenylphosphine (291 mg) in tetrahydrofuran (5 ml) was added diethyl azodicarboxylate (193 mg) under ice-water cooling and the mixture was stirred at 0° C. for 1 hour. After evaporation of solvent, the residue was purified by silica gel column chromatography eluting with a mixture of hexane and ethyl acetate (2:1, 1:1) to give N-(N-t-butoxycarbonyl-N-(2-methoxyethyl)aminosulfonyloxy)succinimide as colorless oil (205 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06967197B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-c30d2af808274ff892df3c9af68590c8 |
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| Source note | uspto-grants-2005_11 |
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