HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594924Generated: November 1, 2026
Allyltrimethylsilane → HCID 21706235, compound
https://huagongshe.com/reaction/1594924
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyltrimethylsilane | HCID 69808 | — |
| Reactant | HCID 21706241 | HCID 21706241 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21706235 | HCID 21706235 | — |
Reaction Steps
Following the procedure described by S. Pansare et al., J. Org. Chem. 1998, 63, 4120-4124, 2-hydroxy-2-(3-methoxy-phenyl)-4-methyl-morpholin-3-one, as described in Step C above, (0.133 g, 0.56 mmol) was dissolved in anhydrous CH2Cl2 (10 mL) under Ar, treated with allyltrimethylsilane (0.534 mL, 3.36 mmol), the mixture cooled to −23° C., then treated with TiCl4 (0.37 mL, 3.36 mmol). After 15 min the reaction mixture was quenched slowly with saturated aqueous NH4Cl solution, left to warm to room temperature, and partitioned between CH2Cl2 and H2O. The aqueous layer was washed with CH2Cl2, the organic layers combined, dried (Na2SO4), filtered and concentrated to dryness to give the title compound after chromatography (SiO2, 0-1% MeOH in CH2Cl2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06284755B1 |
|---|
| Source dataset | uspto-grants-2001_09 |
|---|
| ORD ID | ord-e90635e6eb4a4881877b20a5717bb7b1 |
|---|
| Source note | uspto-grants-2001_09 |
|---|