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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Reactant | 4-(2-((2-Methoxyethoxy)methoxy)ethoxy)aniline | HCID 86724365 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-((2-methoxyethoxy)methoxy)ethoxy)-N-methylaniline | HCID 86724369 | 18.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09126950B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-638493d51b3f4047b86b3f4aa91e1305 |
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| Source note | uspto-grants-2015_09 |
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