HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977913Generated: October 24, 2026
Tetrahydrofuran → Silane, (chloromethyl)(4-ethoxyphenyl)dimethyl-
https://huagongshe.com/en/reaction/977913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Bromophenetole | HCID 68523 | — |
| Reactant | Silane, chloro(chloromethyl)dimethyl- | HCID 74393 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Silane, (chloromethyl)(4-ethoxyphenyl)dimethyl- | HCID 184717 | 49.8% |
Reaction Steps
A mixture of 60 ml of THF, p-bromophenetole (9.7 gram) and chloromethyldimethylsilyl chloride (7.3 gram) was cooled in a dry ice/acetone bath. To the mixture was dropwise added 33 ml of 1.55M n-butyl lithium under an argon atmosphere. After stirring the mixture for additional 15 minutes at -78° C., the stirring was continued at room temperature for 30 minutes. The mixture was added with 6 ml of ethyl acetate and 30 ml of water, and extracted with ethyl ether. The ether extract was washed with saturated sodium chloride solution, dried, and concentrated. Distillation of the residue gave 5.5 gram of chloromethyldimethyl(4-ethoxyphenyl)silane. Physicochemical data of the product is listed in Table 3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04663314 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-b1065096d3b94e748a4c45e61f4fe559 |
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| Source note | uspto-grants-1987_05 |
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