HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442703Generated: October 25, 2026
Diethyl Ether → 3-O-Octadecyl-2-O-tosyl-1-O-tritylglycerol
https://huagongshe.com/reaction/442703
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 1-(Octadecyloxy)-3-(triphenylmethoxy)propan-2-ol | HCID 12896848 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-O-Octadecyl-2-O-tosyl-1-O-tritylglycerol | HCID 13506529 | — |
Reaction Steps
A solution of 1-O-octadecyl-3-O-tritylglycerol (173.51 g, 295.63 mmol) in 895 mL water free pyridine is added to a solution of p-toluenesulfonyl chloride (88.49 g, 464.15 mmol) in 670 mL water-free pyridine with constant stirring. The reaction mixture is kept at ambient temperature (20°-23° C.) for two days. Diethyl ether (2.8 L) is added to this reaction mixture and the organic phase is washed six times with water, twice with diluted aqueous sodium carbonate, and then washed with water until neutral. After drying the organic phase over sodium sulfate, the solvent is removed under reduced pressure. The residue is triturated with isopropanol (1140 mL) with stirring until the product crystallizes. After cooling to 4° C., the product, 1-O-octadecyl-2-O-p-toluenesulfonyl-3-O-tritylglycerol, is isolated by filtration, washed with isopropanol and dried under vacuum.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891881 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-39bf514afbac449c962f4c9b7e1a9336 |
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| Source note | uspto-grants-1999_04 |
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