HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2396821Generated: October 27, 2026
Methyldimethoxysilane → 4-(Methyldimethoxysilyl)butanoic acid terephthalic acid dimethyl ester
https://huagongshe.com/reaction/2396821
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyldimethoxysilane | HCID 85623 | — |
| Reactant | dimethyl N-butenoylaminoterephthalate | HCID 54136524 | — |
| Catalyst | Chloroplatinic acid | HCID 61859 | — |
| Product | 4-(Methyldimethoxysilyl)butanoic acid terephthalic acid dimethyl ester | HCID 86749285 | — |
Reaction Steps
55.5 g (0.2 mol) of dimethyl N-butenoylaminoterephthalate are mixed with 175 mg of hexachloroplatinic acid (as a catalyst) and 85 g (0.8 mol; excess) of methyldimethoxysilane under an inert gas. Gas bubbles which form on the crystals of the catalyst indicate the immediate start of the reaction. The mixture is stirred up at short intervals of time, and after about half an hour is heated to the reflux temperature (about 60° C.) and kept under reflux for 25 hours. The reaction mixture is concentrated down to a deep-brown oil in vacuo. The oil is taken up in 400 ml of n-hexane, whereupon the product crystallizes out in the form of yellow crystals. 4-(Methyldimethoxysilyl)butanoic acid terephthalic acid dimethyl ester)amide is obtained by dissolving in hot n-hexane, crystallization in the cold and drying of the crystals in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05494949 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-f312a55ec65f49078ab591719bbf44ad |
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| Source note | uspto-grants-1996_02 |
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