HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49709Generated: October 29, 2026
2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → t-Butyl 3-acetoxy-5-methyl-4-nitrophenylacetate
https://huagongshe.com/reaction/49709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| Reactant | t-Butyl 3-acetoxy-4-nitrophenylacetate | HCID 18188103 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | t-Butyl 3-acetoxy-5-methyl-4-nitrophenylacetate | HCID 18188096 | — |
Reaction Steps
A stirred solution of t-butyl 3-acetoxy-4-nitrophenylacetate (8.0 g, Reference Example 13) in tetrahydrofuran (350 mL) at −15° C. under argon was treated dropwise with methyl magnesium chloride solution in diethyl ether (7mL, 3M) and after 2 hours a further aliquot of methyl magnesium chloride solution in diethyl ether (7 mL, 3M). After stirring for a further 1 hour the reaction mixture was treated with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (10.4 g), then stirred at room temperature overnight, then partially evaporated and then treated with dichloromethane. The mixture was washed with water, then dried and then evaporated. The residue was subjected to flash chromatography on silica eluting with dichloromethane to give the title compound (1.66 g) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06706738B2 |
|---|
| Source dataset | uspto-grants-2004_03 |
|---|
| ORD ID | ord-acffe975056b4b4b987c21ee70571b50 |
|---|
| Source note | uspto-grants-2004_03 |
|---|