HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074650Generated: October 26, 2026
Water → (-)-1-Benzoyl-2,3-di-p-toluenesulfonyl glycerol
https://huagongshe.com/reaction/1074650
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 1-Monobenzoylglycerol | HCID 137911 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (-)-1-Benzoyl-2,3-di-p-toluenesulfonyl glycerol | HCID 12914086 | 72% |
Reaction Steps
To a solution of 35.5 g (181 mmol) of (-)-1-benzoyl glycerol (G) in 250 ml of dry pyridine at 0° C. is added 83 g (433 mmol) of p-toluenesulfonyl chloride. The mixture is stirred at 0° C. for 15 minutes and then stored in a refrigerator for 144 hours. After cooling the reaction mixture to 0° C., 10 ml of water are added, the mixture is stirred for 10 minutes, and then poured into excess water. The aqueous solution is separated from the gummy product, and extracted with chloroform. The gummy residue is dissolved in chloroform and the combined chloroform solution is washed sequentially with 3 N hydrochloric acid, water, 5% sodium bicarbonate solution, and water. The chloroform solution is dried over Na2SO4 and concentrated under reduced pressure to obtain a solid which, upon recrystallization from absolute ethanol, gives 65.5 g (130 mmol, 72%) of (-)-1-benzoyl-2,3-di-p-toluenesulfonyl glycerol (see Formula (H) in Scheme 2), m.p. 105°-106° C. [α]D2° -22.7 (c, 5.92, CHCl3). 1H NMR (CDCl3) δ8-7 (m, 13H); 4.9 (m, 1H); 4.45 (d, 2H, J=6 Hz); 4.35 (d, 2H, J=5 Hz); 2.42 (s, 3H); 2.38 (s, 3H). 13C NMR (CDCl3) 165.162, 145.136, 133.108, 132.466, 131.649, 129.430, 128.671, 128.087, 127.678, 75.306, 66.899, 61.994, 21.591 ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04393240 |
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| Source dataset | uspto-grants-1983_07 |
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| ORD ID | ord-8ffdabc5f56d4d86a9f7b99d1f9f11ce |
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| Source note | uspto-grants-1983_07 |
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