HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → ethyl (4R)-4-(tert-butoxycarbonylamino)-4-formylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl (4R)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentanoate | HCID 57351319 | — |
| Solvent | Dimethylsulfoxide ethyl acetate | HCID 23053668 | — |
| Product | ethyl (4R)-4-(tert-butoxycarbonylamino)-4-formylbutanoate | HCID 57894011 | 102.6% |
Reaction Steps
Under an atmosphere of argon, to a mixed solution of (4R)-4-t-butoxycarbonylamino-5-hydroxypentanoic acid ethyl ester (1.62 g) and diisopropylethylamine (6.5 ml) in dimethylsulfoxide-ethyl acetate (1:1, 40 mL) was added sulfur trioxide pyridine complex (2.96 g) in ice bath and the mixture was stirred in ice bath for 1 hour. The reaction solution was poured into ice water and extracted with ethyl acetate. The organic layer was washed with 0.5N hydrochloric acid, water and brine, dried over anhydrous magnesium sulfate and concentrated to give the title compound (1.65 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08026273B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-5362cd58179f4effa83789ce8ce6c3a4 |
| Source note | uspto-grants-2011_09 |