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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2274302Generated: October 30, 2026

Formaldehyde → 4-(2-((2-methoxyethoxy)methoxy)ethoxy)-N-methylaniline

https://huagongshe.com/reaction/2274302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl acetate hexaneHCID 21226206—
Reactant4-(2-((2-Methoxyethoxy)methoxy)ethoxy)anilineHCID 86724365—
SolventWaterHCID 962—
Product4-(2-((2-methoxyethoxy)methoxy)ethoxy)-N-methylanilineHCID 8672436918.9%

Reaction Steps

To a 25 mL, 3-neck RBF equipped with a magnetic stirrer and calcium chloride guard tube, 4-(2-((2-methoxyethoxy)methoxy)ethoxy)aniline (1.0 g in 10 mL DMF) and formaldehyde (0.062 g) were added portion wise to the reaction mixture at 0° C. and stirred for an additional 10 minutes. NaBH(OAc)3 (0.88 g) was added and the mixture was stirred for 5 minutes. The reaction was monitored on TLC using hexane:ethyl acetate (5:5) as mobile phase. After completion of the reaction, the reaction mixture was poured in water and extracted with ethyl acetate. Organic layer was washed with brine, dried over sodium sulfate and concentrated completely under reduce pressure at 40° C. Crude material was purified by using column chromatography. Desired product was eluted with 7% ethyl acetate in hexane to give 0.200 g of 4-(2-((2-methoxyethoxy)methoxy)ethoxy)-N-methylaniline. M+1=256.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09126950B2
Source datasetuspto-grants-2015_09
ORD IDord-638493d51b3f4047b86b3f4aa91e1305
Source noteuspto-grants-2015_09