HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl acetate hexane → HCID 66648815, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | HCID 59706497 | HCID 59706497 | — |
| Reactant | Trimethylsilyldiazomethane hexane | HCID 86587183 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66648815 | HCID 66648815 | 98% |
Reaction Steps
To a solution of 2-[4-(t-butyldimethylsilyloxy)benzyl]-3-isopropylmaleic anhydride (823 mg, 2.28 mmol) in methanol (15 mL) was added a 2.0 M trimethylsilyl diazomethane-hexane solution (8.5 mL, 17 mmol) with stirring at room temperature. After stirring at room temperature for 30 min, the reaction mixture was concentrated under reduced pressure and the residue thus obtained was subjected to silica gel column chromatography (hexane-ethyl acetate 10:1→8:1) to give 913 mg of dimethyl 2-[4-(t-butyldimethylsilyloxy)benzyl]-3-isopropylmaleate as oil (yield: 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09260375B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-64111429f7184c26bd3b0dce3645aeae |
| Source note | uspto-grants-2016_02 |