HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorodimethylsilane → 7-{2-[Chloro(dimethyl)silyl]propoxy}-4-methyl-2H-1-benzopyran-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorodimethylsilane | HCID 66108 | — |
| Reactant | 7-(Allyloxy)-4-methyl-2H-chromen-2-one | HCID 238952 | — |
| Catalyst | Chloroplatinic acid | HCID 61859 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-{2-[Chloro(dimethyl)silyl]propoxy}-4-methyl-2H-1-benzopyran-2-one | HCID 19821061 | — |
Reaction Steps
To a solution of 2.16 g of 7-allyloxy-4-methylcoumarin and 5×10-6 mols chloroplatinic acid hydrosilylation catalyst in 20 ml toluene was slowly added 2.0 g of Me2SiHCl and the mixture was heated at 40°-42° for 6 hrs. Toluene and unreacted silane were then removed at reduced pressure to yield 7{2-(chlorodimethylsilyl)propoxy}-4-methylcoumarin. The 1H-NMR spectrum (ppm) contained signals at 0.2(s) for SiCH3, (6H); 2.4(s) for CH3,(3H); 4.0(t) for CH2O, (2H) and no signal for the allyl moiety.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05107008 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-38e12346233a4e4599a3ce6c0408381d |
| Source note | uspto-grants-1992_04 |