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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298792Generated: October 25, 2026

Pyridine → 1-o-t-Butyldimethylsilyl-2-o-methyl-3-o-oleoyl-rac-glycerol

https://huagongshe.com/reaction/2298792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantOleoyl chlorideHCID 5364783—
Reactant1-o-t-Butyldimethylsilyl-2-o-methyl-rac-glycerolHCID 22316451—
SolventDichloromethaneHCID 6344—
Product1-o-t-Butyldimethylsilyl-2-o-methyl-3-o-oleoyl-rac-glycerolHCID 8775954399%

Reaction Steps

To a solution of alcohol Compound 42 (1.1 g, 5.0 mmol) in CH2Cl2 (10 mL) was added oleoyl chloride (1.8 mL, 5.5 mmol) followed, after 5 min, by the addition of pyridine (0.44 mL, 5.5 mmol). After TLC analysis indicated that the reaction had gone to completion, the mixture was partitioned between ethyl acetate (100 mL) and H2O (30 mL), the organic extract was dried (MgSO4) and concentrated to give 1-O-t-butyldimethylsilyl-2-O-methyl-3-O-oleoyl-rac-glycerol (Compound 43) (2.4 g, 99%) as a dark brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495532B1
Source datasetuspto-grants-2002_12
ORD IDord-f38b2a6bd4cf4c29b600628ea5e3d8de
Source noteuspto-grants-2002_12