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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650461Generated: October 28, 2026

Triethanolamine → HCID 21872526, compound

https://huagongshe.com/reaction/650461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethanolamineHCID 7618—
ReactantTetrahydrofuranHCID 8028—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
Reactant1-[(Chloromethoxy)methoxy]-2-methoxyethaneHCID 13128699—
ReactantPotassium tert-butoxideHCID 23665647—
SolventMethanolHCID 887—
ProductHCID 21872526HCID 2187252670%

Reaction Steps

To a suspension of 135.3 grams of potassium t-butoxide in 900 ml of tetrahydrofuran, 50.0 grams of triethanolamine in 100 ml of tetrahydrofuran was added dropwise over 10 minutes while stirring under ice cooling. After 40 minutes of stirring, 150.4 grams of chloromethyl 2-methoxyethyl ether was added dropwise over 30 minutes while continuing stirring under ice cooling. After 30 minutes of stirring, 37.6 grams of potassium t-butoxide was added while continuing stirring under ice cooling. After 20 minutes of stirring, 41.8 grams of chloromethyl (2-methoxyethoxy)methyl ether was added dropwise over 10 minutes while continuing stirring under ice cooling. After 40 minutes of stirring, 250 ml of methanol was added. After 30 minutes of stirring, the reaction solution was filtered with a sufficient amount of Celite, and the residue was washed with ether. The filtrate was concentrated under vacuum, and the resulting oily matter was dissolved in 2,000 ml of methylene chloride. Using a separatory flask, the solution was washed three times with 200 ml of water. The organic phase was concentrated in vacuum. On analysis by 1H-NMR, the resulting oily matter was found to be tris[2-(2-methoxyethoxy)-methoxyethyl]amine, designated Amine 2. Amount 103.9 grams, yield 70.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274286B1
Source datasetuspto-grants-2001_08
ORD IDord-4fe3e45a710740a4aa88b1126655e625
Source noteuspto-grants-2001_08