HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → tert-butyl N-(5-formyl-1,3-thiazol-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Reactant | Tert-butyl 5-(hydroxymethyl)thiazol-2-ylcarbamate | HCID 53397352 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl N-(5-formyl-1,3-thiazol-2-yl)carbamate | HCID 53393345 | — |
Reaction Steps
To a solution of compound 62.2 (18.5 mmol) in dichloromethane is added molecular sieves (4.0 g) and PDC (39.0 mmol) at room temperature (THF is added to help dissolve the starting material). After 1.5 hours, an additional equivalent of PDC is added and the reaction is stirred for 5.5 hours. The reaction mixture is poured directly onto a silica gel column and is eluted with a gradient of 100% dichloromethane to 100% EtOAc. Fractions containing the desired product are pooled and concentrated to afford (5-formyl-thiazol-2-yl)-carbamic acid tert-butyl ester (compound 62.3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601725B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-6c5cab683b3c441fbfc686c9d6fa5311 |
| Source note | uspto-grants-2009_10 |