HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180563Generated: November 1, 2026
HCID 22490925, compound → HCID 22491008, compound
https://huagongshe.com/reaction/2180563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22490925 | HCID 22490925 | — |
| Reactant | HCID 178461633 | HCID 178461633 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Product | HCID 22491008 | HCID 22491008 | — |
Reaction Steps
To a solution of 8-tert-butyl-3-ethoxy-5,5-dimethyl-5,6-dihydro-naphthalene-2-carbaldehyde (Compound A-27, 450 mg, 1.57 mmol) in THF (7 mL) and 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU, 0.3 mL) was added ethylmagnesium chloride (2 M in THF, 1.6 mL, 3.1 mmol). After stirring at 0° C. for 30 min, the reaction was quenched with 1N HCl. The resulting mixture was diluted with water, extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried (MgSO4), filtered, and concentrated under reduced pressure to give the title compound as a colorless oil after purification by flash chromatography (silica gel, 10% ethyl acetate in hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06887896B1 |
|---|
| Source dataset | uspto-grants-2005_05 |
|---|
| ORD ID | ord-9aa1a6af77ca4e1f8f9dbe764bfef81a |
|---|
| Source note | uspto-grants-2005_05 |
|---|