HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231342Generated: October 26, 2026
Aminopropyltrimethoxysilane → HCID 14388383, compound
https://huagongshe.com/reaction/2231342
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aminopropyltrimethoxysilane | HCID 83756 | — |
| Reactant | Methanol tert-butyl alcohol | HCID 19609033 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 14388383 | HCID 14388383 | 94% |
Reaction Steps
Into a 500 ml 3-necked flask equipped with a magnetic stirrer, heating mantle, thermometers, a 12 in. distilling column packed with 1/8 in. glass helices, addition funnel, distilling head and receiver was added 179.3 g (1.0 mole) of 3-aminopropyltrimethoxysilane. The flask was heated to 160° C. and from the (heated) addition funnel 160 g (2.16 moles) of t-butanol was slowly added with the simultaneous distillation of methanol/t-butanol to the receivers. The rate of addition of t-butanol was kept slow in order to maintain as high a flask temperature as possible (150°-170° C). Periodic sampling of the flask and lites for gas chromotograph analysis indicated that after 2.16 moles t-butanol had been added, approximately an 80% conversion of 3-aminopropyltrimethoxysilane to Compound A* had been achieved. Distillation of this material with four cuts (94°-100° C. at 20 mm Hg) produced 100 g of 94% pure aminopropyl-t-butoxydimethoxysilane (combined cuts 2, 3, 4). Cut one, enriched in 3-aminopropyltrimethoxysilane was 30 grams.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04782102 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-3768c0e51c2143c2bac031a033bd372b |
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| Source note | uspto-grants-1988_11 |
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