HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470163Generated: October 29, 2026
Hydrochloric Acid → tert-Butyl 12-hydroxy-4,7,10-trioxadodecanoate
https://huagongshe.com/reaction/1470163
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylene Glycol | HCID 8172 | — |
| Reactant | tert-Butyl acrylate | HCID 15458 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Catalyst | Sodium | HCID 5360545 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl 12-hydroxy-4,7,10-trioxadodecanoate | HCID 3625858 | 88.4% |
Reaction Steps
To triethyleneglycol (17.6 g, 117.20 mmol, 3.00 equiv) in anhydrous THF (70 mL), was added sodium (30 mg, 1.25 mmol, 0.03 equiv). Tert-butyl acrylate (5.0 g, 39.01 mmol, 1.00 equiv) was added after the sodium had dissolved. The resulting solution was stirred overnight at room temperature and then neutralized with 1.0 N hydrogen chloride. After removal of the solvent, the residue was suspended in 50 mL of brine and extracted with 3×50 mL of ethyl acetate. The combined organic layers were washed with saturated brine and dried over anhydrous sodium sulfate. After evaporation of the solvent, the tert-butyl 3-(2-(2-(2-hydroxyethoxy)ethoxy)ethoxy)propanoate (9.6 g) was isolated as a colorless oil, which was used directly for the next reaction step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09006281B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-1f7500ac46074c749545cfddac7f8e3b |
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| Source note | uspto-grants-2015_04 |
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