HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 886687Generated: October 31, 2026
Triethylamine → 1,3-Bis(benzyloxy)propan-2-one
https://huagongshe.com/reaction/886687
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Bis(benzyloxy)propan-2-ol | HCID 247614 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1,3-Bis(benzyloxy)propan-2-one | HCID 11391582 | 75.8% |
Reaction Steps
A mixture of sulfur trioxide/pyridine complex (2.33 g, 4 equivalents) in DMSO (3 ml) and triethylamine (2.05 ml, 4 equivalents) was stirred to give a pale yellow solution. To this was added a solution of 1,3-dibenzyloxy-2-propanol (1 g) in DMSO (1 ml) over 2 minutes. (The reaction mixture was kept in a water bath). The temperature of the reaction mixture reached 30° C. After 10 minutes the water bath was removed and the reaction mixture was stirred at room temperature (ca 20-25° C.) for 3 hours. The reaction mixture was diluted with ethyl acetate (15 ml) and water (15 ml), stirred and the organic extract was separated. The organic extract was washed with 5% w/v sodium chloride (2×10 ml) and water (10 ml). The separated organic extract was concentrated in vacuo to give an oil which solidified to provide 0.75 g of 1,3-dibenzyloxy-2-propanone in 75.8% yield. An NMR spectrum of product was concordant with a reference sample.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247377B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-b250760bb752490a8f7d02fdbbdadcb4 |
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| Source note | uspto-grants-2012_08 |
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