HuagongsheHuagongshe Chemistry Print Report · For research reference only
Maleic Anhydride → 5-(Trimethoxysilyl)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | (Buta-1,3-dien-2-yl)(trimethoxy)silane | HCID 13330888 | — |
| Product | 5-(Trimethoxysilyl)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione | HCID 13330893 | 85% |
Reaction Steps
To 0.36 g (2.1 mmol) of 2-(trimethoxy)silyl-1,3-butadiene [II], were added 0.19 g (1.9 mmol) of maleic acid anhydride [III]at room temperature and stirred for one hour. After the reaction was over, the reaction product was separated on chromotography using silica gel and developing with a mixed solvent of n-hexane-diethyl ether to obtain 0.44 g of 4-(trimethoxy)silyl-1,2,3,6-tetrahydrophthalic acid anhydride [I](yield: 80 %, liquid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04837339 |
| Source dataset | uspto-grants-1989_06 |
| ORD ID | ord-2577caf040d845b491ffbe8e9ef367f5 |
| Source note | uspto-grants-1989_06 |