HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → Tert-butyl but-3-EN-1-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Di-tert-butyl N-3-butenyliminodicarboxylate | HCID 12186469 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl but-3-EN-1-ylcarbamate | HCID 11263760 | 96.2% |
Reaction Steps
To a solution of 186 (708 mg, 2.60 mmol) in DCM (20 mL) was added trifluoroacetic acid (593 mg, 5.20 mmol) and the mixture was allowed to stir for 5 min before being quenched with 2M NaOH (25 mL) and extracted with DCM (3×20 mL). The combined organic fractions were dried, and concentrated to yield the title compound (429 mg, 2.50 mmol, 96%) as a light brown oil, which had spectral data in agreement with that reported.104 1H NMR (CDCl3, 300 MHz): δ 5.75 (m, 1H, H3); 5.08 (m, 2H, H4); 4.59 (bs, 1H, NH); 3.20 (dd, J=6.3, 12.6 Hz, 2H, H1); 2.24 (dd, J=6.9, 12.6 Hz, 2H, H2); 1.44 (s, 9H, (CH3)3). Mass Spectrum (ES, +ve) m/z 116 (100%) [MH+ less 56 (Boc rearrangement].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039430B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-9d001b085c4645b983ea29c8d3fe6312 |
| Source note | uspto-grants-2011_10 |