HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252671Generated: October 30, 2026
Imidazole → 1-Palmitoyl-3-t-butyldimethylsilyl-glycerol
https://huagongshe.com/reaction/252671
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 1-Monopalmitin | HCID 14900 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Palmitoyl-3-t-butyldimethylsilyl-glycerol | HCID 85395614 | 100% |
Reaction Steps
1-palmitoyl-glycerol (33.0 g), dichloromethane (330 ml) and imidazole (13.6 g) were added into 1 L reactor, and the reaction mixture was cooled to 0° C. Then, t-butyl-dimethylsilylchloride (18.0 g) was added, and the reaction mixture was stirred for 2 hours. After filtering the reaction mixture, the solvent was removed by distillation under reduced pressure, and purified water (165 ml) and heptane (150 ml) were added for an extraction. The separated organic layer was extracted with purified water (80 ml) again, and then the organic layer was dehydrated with anhydrous MgSO4, and filtered. Then, the solvent was removed by distillation under reduced pressure to obtain 1-palmitoyl-3-t-butyldimethylsilyl-glycerol (yield: 100%) {1H NMR (400 MHz, CDCl3): δ 0.78-0.83 (m, 18H), 1.18-1.31 (m, 24H), 1.50-1.56 (m, 2H), 2.24 (t, 2H), 3.51-3.60 (m, 2H), 3.76-3.79 (p, 1H), 4.01-4.10 (m, 2H)}.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868196B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-20a7c72a83ef44bbb45614e8e4beb78a |
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| Source note | uspto-grants-2011_01 |
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