HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876580Generated: October 30, 2026
Dimethylformamide → HCID 67222560, compound
https://huagongshe.com/reaction/876580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 1-(1,1-Dimethylethyl) (2R,3R)-2,3-bis(acetyloxy)butanedioate | HCID 14143476 | — |
| Reactant | HCID 65029835 | HCID 65029835 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67222560 | HCID 67222560 | 102.8% |
Reaction Steps
To a solution of (R,R)-2,3-bis(acetyloxy)-butanedioic acid mono tert-butyl ester (3.25 g: Tetrahedron, 45, 3071-3080, 1989) in CH2Cl2 (65 mL), were added oxalyl chloride (1.06 mL) and DMF (50 microL) at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes then pyridine (3.82 mL) was added into the mixture at the same temperature. The reaction mixture was stirred at the same temperature for 5 minutes. To the mixture, was added a solution of compound 54-2 (2.5 g) in CH2Cl2 (12.5 mL) at 0° C. The mixture was stirred for 1 hour at the same temperature. Then the mixture was concentrated in vacuo and the resulting residue was suspended in water. The mixture was extracted with EtOAc and the organic layer was washed with 1N HCl aq., sat. NaHCO3 aq., brine, and it was dried with anhyd. Na2SO4. The solvent was removed under reduced pressure to obtain compound 54-3 (5.7 g) as brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08987242B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-b2e63aaab69c415a93f2fd1ba5763133 |
|---|
| Source note | uspto-grants-2015_03 |
|---|