HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Tert-butyl 6-formylchroman-4-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 68930912 | HCID 68930912 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 6-formylchroman-4-ylcarbamate | HCID 86598502 | — |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
(6-Bromo-chroman-4-yl)-carbamic acid tert-butyl ester (3.859 g, 11.76 mmol) was dissolved in THF (50 mL) and cooled to −78° C. n-Butyllithium (2.5 M) (11.76 mL, 29.40 mmol) was added drop-wise to the stirred solution. The reaction mixture was stirred at −78° C. for 30 min and DMF (4.55 mL, 58.8 mmol) was added drop-wise and the system was slowly warmed to RT overnight. The reaction was quenched with saturated aqueous NH4Cl solution and extracted with EtOAc. The combined organics were dried with MgSO4 and concentrated in vacuo to afford the crude compound, which was purified by flash column chromatography to furnish the pure title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07199244B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-29f87b07152a47a9aadbbe466a843f71 |
| Source note | uspto-grants-2007_04 |