HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270656Generated: October 25, 2026
Diisopropylamine → 2-[2-(2-Methoxyethoxymethoxy)ethyl]thiophene
https://huagongshe.com/reaction/270656
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| Reactant | 2-Thiopheneethanol | HCID 79400 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[2-(2-Methoxyethoxymethoxy)ethyl]thiophene | HCID 57710061 | 85% |
Reaction Steps
15.0 g of 2-thiopheneethanol was dissolved in 350 mL of dichloromethane, and 30.2 g of diisopropylamine was added thereto. The resulting mixture was cooled to 0° C. and 17.5 g of 2-methoxyethoxymethyl chloride was added thereto. The resulting mixture was stirred for 2 hours and heated to reflux for 2 hours. The reaction product solution was cooled and concentrated by evaporation under reduced pressure. To the residue, 200 mL of water and 250 mL of n-hexane were added, and the resulting mixture was stirred for 5 minutes. Aqueous layer was discarded, and the organic layer was washed twice with 700 mL portions of water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to obtain 21.5 g (yield of 85%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07449580B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-e81fb2b8b6d84ee4beb9aff279930772 |
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| Source note | uspto-grants-2008_11 |
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