HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179101Generated: October 31, 2026
Butyl glycidyl ether → HCID 22141571, compound
https://huagongshe.com/reaction/1179101
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl glycidyl ether | HCID 17049 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium hydrosulfide | HCID 28015 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 22141571 | HCID 22141571 | — |
Reaction Steps
A solution of butyl glycidyl ether (2.91 g, 22.39 mmol) in isopropanol (5 mL) and H2O (1 mL) was added to sodium bisulfide (0.628 g, 11.20 mmol) under nitrogen in a 100 mL 3-neck round bottom flask equipped with a N2 inlet, a rubber septum, glass stopper and a magnetic stir bar. The mixture was heated at 90° C. and monitored for completion by gas chromatography/mass spectrometry for disappearance of starting materials and formation of the product. After 3 h, the reaction was judged to be complete. The mixture was cooled to ambient temperature and treated with saturated NH4Cl (5.0 mL) and extracted into ethyl acetate (50 mL). The solvent was dried (MgSO4), filtered, and evaporated in-vacuo to give the product, 1,1′-thiobis(3-butoxypropan-2-ol), which was identified by mass spectrometry as well as 1H and 13C NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07279447B2 |
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| Source dataset | uspto-grants-2007_10 |
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| ORD ID | ord-2edbd6c266bb44dbaf5fbf7f86c9a06c |
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| Source note | uspto-grants-2007_10 |
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