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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446649Generated: October 29, 2026

Acetone → HCID 131730695, compound

https://huagongshe.com/reaction/446649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 131730696HCID 131730696—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 131730695HCID 131730695—

Reaction Conditions

Temperature-71 °C

Reaction Steps

10.5 ml of n-BuLi as a 1.6M solution in hexane are added dropwise to 4.32 g of 1-bromo-3,5-bis[(tert-butyl)dimethylsilanyloxymethyl]benzene (G. T. Crisp and P. D. Turner, Tetrahedron, 2000, 56 (42), 8335) in solution in 150 ml of THF cooled to −71° C. After 1 h 30, 4.27 ml of acetone are added dropwise. The mixture is allowed to return to AT and then hydrolysed with a saturated aqueous NH4Cl solution. The aqueous phase is extracted with 100 ml of AcOEt, the combined organic phases are dried over MgSO4 and concentrated under RP, and the residue is purified by flash chromatography on silica (Biotage 65+M) using a gradient from 0 to 20% AcOEt in heptane. 2.48 g of 1-(1-hydroxy-1-methylethyl)-3,5-bis[(tert-butyl)dimethylsilanyloxymethyl]benzene are thus obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481042B2
Source datasetuspto-grants-2013_07
ORD IDord-2c75fe631e4c4c39a0b66003a78e5d79
Source noteuspto-grants-2013_07