HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879427Generated: November 1, 2026
Ethylenediamine → 4-[(Triethoxysilyl)methyl]morpholine
https://huagongshe.com/reaction/1879427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Silane, (chloromethyl)triethoxy- | HCID 84858 | — |
| Product | Morpholine | HCID 8083 | 45% |
| Product | 4-[(Triethoxysilyl)methyl]morpholine | HCID 12419881 | 74.2% |
Reaction Steps
82 g of dry morpholine (pKb 5.67) were heated to 120° C. in a 500 ml four-necked flask having a reflux condenser, KPG stirrer and thermometer and 80 g of chloromethyltriethoxysilane were added in the course of 180 min with stirring. After the end of the addition, the temperature was reduced to 105° C. and 226.6 g of ethylenediamine (pKb 4.07) were added to the mixture in the course of 10 min with stirring, phase separation occurring. At constant temperature, stirring was effected for a further 30 min and the heavier ethylenediamine hydrochloride phase was then separated off. The upper phase was subjected to fractional distillation without a distillation column. 37 g (45% recovery) of morpholine having a purity of 89.7% and 73.5 g (yield 74.2%) of 4-(triethoxysilylmethyl)-tetrahydro-1,4-oxazine were obtained, the purity of which was determined as 97.3%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314263B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-2112643ff15446519237a9eeddb63b23 |
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| Source note | uspto-grants-2012_11 |
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