HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727247Generated: October 30, 2026
Chlorotrimethylsilane → HCID 10313521, compound
https://huagongshe.com/reaction/727247
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | 3-Furaldehyde | HCID 10351 | — |
| Reactant | 4-Methylthiazole | HCID 12748 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10313521 | HCID 10313521 | — |
Reaction Steps
4-Methylthiazole (3g) in dry diethyl ether was added dropwise to a stirred solution of n-butyllithium (1.6M in hexanes, 21ml) in diethyl ether (20ml) at -78° C. under an atmosphere of dry nitrogen. After 30 minutes, trimethylsilylchloride (3.9ml) was added and the mixture was then allowed to warm to 0° C. The mixture was then cooled to -78° C. and further n-butyllithium (21ml) was added. The mixture was warmed to 0° C. After 30 minutes the mixture was again cooled to -78° C. and 3-furaldehyde (5g) in diethyl ether (10ml) was added. The mixture was allowed to warm to room temperature and after 30 minutes saturated aqueous sodium hydrogen carbonate was added. The reaction mixture was extracted with diethyl ether in the usual manner to give the crude product which was then purified by flash chromatography on silica gel to give the title compound. M.p. 44°-46° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05712299 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-29809dfebc654c1fa0cbb8c7df62b65d |
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| Source note | uspto-grants-1998_01 |
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