HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977284Generated: October 30, 2026
Triethylamine → (+/-)-1-S-hexadecyl-2-O-methyl-3-O-mesylthioglycerol
https://huagongshe.com/reaction/977284
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-(Hexadecylsulfanyl)-2-methoxypropan-1-ol | HCID 14522776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+/-)-1-S-hexadecyl-2-O-methyl-3-O-mesylthioglycerol | HCID 14522778 | 89% |
Reaction Steps
To a solution of 3.0 grams (0.009 mole) (±)-1-S-hexadecyl-2-O-methylthioglycerol in 200 milliliters of DCM and 1.0 milliliter (0.010 mole) of triethylamine was added 1.2 grams (0.012 mole) of methanesulfonyl chloride and the reaction stirred at room temperature for 24 hours. The reaction mixture was then extracted twice with 200 milliliter portions of water, twice with 200 milliliter portions of 5% HCl, once with 200 milliliters of saturated NaHCO3, and once with 200 milliliters of brine. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated in vacuo to yield 3.4 grams (89%) of a colorless oily residue. 1H-NMR (CDCl3): delta, 0.87(t, 3H, terminal methyl), 1.2-1.6[m, 28H, (CH2)14 ], 2.58(m, 2H, S--CH2), 2.62(m, 2H, CH--CH2 --S), 3.08(s, 3H, SO2 --CH3), 3.40-3.50(m, 4H, CH, CH3 --O), 4.35 (m, 2H, CH2 --OSO2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05614548 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-b08f4d519b1d4390a4c00a9d48497241 |
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| Source note | uspto-grants-1997_03 |
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