HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651652Generated: October 26, 2026
1-(Chloromethoxy)-2-methoxyethane → 2-[1-(Methoxyethoxymethoxy)ethyl]-3-methylthiothiophene
https://huagongshe.com/reaction/1651652
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(1-Hydroxyethyl)3-methylthiothiophene | HCID 23050277 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[1-(Methoxyethoxymethoxy)ethyl]-3-methylthiothiophene | HCID 54105652 | 87.1% |
Reaction Steps
To a stirred solution of 2-(1-hydroxyethyl)3-methylthiothiophene (13.5 g, 0.077 mol) in dry methylene chloride (100 ml) was added methoxyethoxymethyl chloride (11.5 g, 0.092 mol) followed by N,N-diisopropylethylamine (12.1 g, 0.092 mol) with cooling. The solution was stirred at room temperature for 18 hours. Some starting material remained upon work up at this point. The material was recycled as above using 1/2 the above quantities of methoxyethoxymethyl chloride and N,N-diisopropylethyl amine. After 5 hours at room temperature the reaction was completed. The solution was washed with water, dilute HCl, saturated NaHCO3 solution and again with water. Then it was dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Pure product was obtained as a yellow oil (17.6 g, 87%). TLC confirmed the purity and NMR and mass spectrometry (M/Z=262) supported the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04929637 |
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| Source dataset | uspto-grants-1990_05 |
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| ORD ID | ord-f59b579c31c041e8baf034b25603ad51 |
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| Source note | uspto-grants-1990_05 |
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