HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16215Generated: October 25, 2026
2-Butene-1,4-diol → 4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-ol
https://huagongshe.com/reaction/16215
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Butene-1,4-diol | HCID 8065 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-ol | HCID 66656949 | — |
Reaction Steps
NaH (3 g, 75 mmol, 60% in oil) was added portion-wise to a stirred and cooled (0° C.) solution of but-2-ene-1,4-diol (6 g, 68.09 mmol) in dry tetrahydrofuran (250 mL). After the addition, the mixture was allowed to warm to room temperature and stirred for another two hours. The resulting white mixture was then cooled (0° C.) and tert-butyl-chlorodiphenylsilane (15.7 mL, 61.28 mmol) was added drop wise. After twenty minutes, the cooling bath was removed and the mixture was allowed to stir overnight at room temperature. Saturated NH4Cl was poured into the reaction mixture and the reaction was partitioned with diethyl ether (200 mL). The organic layer was washed with brine, dried (MgSO4), and filtered. The resulting oil was used in the following step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737137B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-cacae96a195b4eb7a82169604af3d677 |
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| Source note | uspto-grants-2010_06 |
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