HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865784Generated: October 26, 2026
Potassium Carbonate → 2,3-Di-(2-methoxy ethoxy)propanol
https://huagongshe.com/reaction/865784
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4,7,10,13,16-Hexaoxacyclooctadecane-2-methanol | HCID 3611393 | — |
| Reactant | Borate(1-), tetrafluoro-, hydrogen, compd. with 1,1'-oxybis(ethane) (1:1:1) | HCID 16211330 | — |
| Reactant | 1-Tert-butyloxy-2,3-di-(2-methoxy ethoxy)propane | HCID 23374671 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Di-(2-methoxy ethoxy)propanol | HCID 23374667 | — |
Reaction Steps
Compound 29 was prepared by a method similar to that described by Montanari and Tundo20 for the synthesis of 2-(hydroxy methyl)-1,4,7,10,13,16-hexaoxacyclooctadecane. KBF4 complex, (2-(hydroxy methyl)-18-crown-6). To a solution of compound 23 (10.0 g, 0.038 mol.) in dichloromethane (100 ml) was added tetrafluoroboric acid-diethyl ether complex (54% in diethyl ether), (13.7 ml). The mixture was left stirring at room temperature for 20 minutes. The acid was neutralized with solid potassium carbonate, inorganic salts were filtered, the solvent was removed by rotary evaporation to give a pale yellow oil. The crude product was distilled under vacuum (bpt. 94°-95° C., 0.02 torr) to give a colorless liquid (18.75 g, 78%): 1H-NMR (CDCl3), d (ppm) 3.5-3.9 (m, 13H), 3.35-3.4 (s, 6H), 2.75-2.8 (s, 1H); 13C-NMR (CDCl3), d (ppm) 79.56, 72.07, 71.73, 71.16, 70.59, 69.35, 62.40, 58.83, 58.75.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05567783 |
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| Source dataset | uspto-grants-1996_10 |
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| ORD ID | ord-9b03a1ab8e694ed5876b997afc9e5a94 |
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| Source note | uspto-grants-1996_10 |
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