Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Trimethylsilyl)ethanol | HCID 18013 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 34180170 | HCID 34180170 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 42643275 | HCID 42643275 | 67.2% |
Reaction Steps
40.1 (3R,4R)-Pyrrolidine-1,3,4-tricarboxylic acid 1-tert.-butyl ester 3-ethyl ester (CAS 595556-31-35 g; 17 mmol) was dissolved in toluene (50 ml), triethylamine (2.43 ml; 17 mmol) and diphenylphosphoryl azide (3.77 ml; 17 mmol) were added. The reaction mixture was stirred at 80° C. for 30 min. After that 2-(trimethylsilyl)ethanol (12.41 ml; 87 mmol) was added and the reaction mixture was stirred at 90° C. for 14 h. The reaction mixture was evaporated, dissolved in ethyl acetate and extracted with aqueous Na2CO3 and aqueous HCl (1N). The organic layers were combined and dried over Na2SO4. Flash chromatography over silica gel using DCM/MeOH/NH3 as eluent yielded 4.6 g (65.6%) (3S,4R)-4-(2-trimethylsilanyl-ethoxycarbonylamino)-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester. MS 403.5 [M+H+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820699B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-a82ddb0237da4def9f9bd1357179f5c7 |
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| Source note | uspto-grants-2010_10 |
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