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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(Hexadecylsulfanyl)-2-methoxypropan-1-olHCID 14522776—
SolventDichloromethaneHCID 6344—
Product(+/-)-1-S-hexadecyl-2-O-methyl-3-O-mesylthioglycerolHCID 1452277889%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05614548
Source datasetuspto-grants-1997_03
ORD IDord-b08f4d519b1d4390a4c00a9d48497241
Source noteuspto-grants-1997_03