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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Butene-1,4-diolHCID 8065—
ReactantSodium hydrideHCID 24758—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
SolventTetrahydrofuranHCID 8028—
Product4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-olHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737137B2
Source datasetuspto-grants-2010_06
ORD IDord-cacae96a195b4eb7a82169604af3d677
Source noteuspto-grants-2010_06