HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl acetate → 3-(Triphenylsilyl)propan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl acetate | HCID 11584 | — |
| Reactant | Triphenylsilane | HCID 69922 | — |
| Product | 3-(Triphenylsilyl)propan-1-ol | HCID 4060335 | — |
Reaction Steps
The above-mentioned compounds (G-1), (G-2) and (G-3) are prepared by hydrolyzing an adduct (C) of commercially available triphenylsilane (A) and allyl acetate (B) with an alkali to obtain 3-hydroxypropyltriphenylsilane (D) and reacting this compound (D) with acryloyl chloride (E), methacryloyl chloride (E-2) or allyl chloroformate (E-3) in the presence of a dehydrochlorinating agent such as pyridine or triethylamine. ##STR5##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04742136 |
| Source dataset | uspto-grants-1988_05 |
| ORD ID | ord-200b6f90d7334ae683603ecc04a4598c |
| Source note | uspto-grants-1988_05 |