HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 654968Generated: October 30, 2026
Acetic Anhydride → HCID 19885938, compound
https://huagongshe.com/reaction/654968
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15663251 | — |
| Reactant | HCID 15728720 | HCID 15728720 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 19885938 | HCID 19885938 | — |
Reaction Steps
A solution of 2-methoxyethoxymethyl tributylstannylmethyl ether (620 mg, 1.5 mmole) in tetrahydrofuran (THF) (5 ml) at -78° C. was treated with n-butyl lithium (a 2.5M solution in hexane: 0.67 ml, 1.67 mmole). After 10 min., a solution of 5-trimethylsilyl-3-furaldehyde (254 mg, 1.5 mmole) in THF (2 ml) was added. The solution was stirred for 3 hours while the cooling bath warmed to room temperature. Acetic anhydride (309 mg, 3.03 mmole) was added and the solution stirred at room temperature overnight. The mixture was quenched with water and the aqueous phase extracted with ethyl ether. The combined organic portions were dried over MgSO4, filtered and concentrated. Purification by flash chromatography (silica, 50% ethyl ether/hexane) gave the title compound as a light yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05134128 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-eb6a66dd789f48f9bd0f521e7a68aeca |
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| Source note | uspto-grants-1992_07 |
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