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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926553Generated: November 4, 2026

tert-Butyldimethylsilyl chloride → HCID 11367157, compound

https://huagongshe.com/reaction/1926553

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 46900816HCID 46900816—
ReactantHCID 178506908HCID 178506908—
SolventAcetoneHCID 180—
ProductHCID 11367157HCID 1136715741%

Reaction Steps

Following the general procedure for the preparation of acetylsilanes (see Example 1) tert-butyl(1-hydroxy-1-methylethyl)dimethylsilane was prepared from tert-butylchlorodimethylsilane (5.00 g, 33.2 mmol) and ethoxyvinyl lithium (prepared from ethyl vinyl ether (3.11 g, 43.1 mmol) and tert-butyl lithium (1.9 M in pentane, 22.7 ml, 43.1 mmol) in THF (50 ml)). The crude material was hydrolysed with acetone/1 N HCl (2:1, 60 ml), and purified by silica-gel chromatography (silica-gel 40-63 μm, hexane/EtOAc, 9:1) to afford 2.13 g (41% over 2 steps) of acetyl(tert-butyl)dimethylsilane, of which 1.44 g, (9.10 mmol) was reacted according to Example 1 with methyl lithium (1.6 M in Et2O, 28.4 ml, 45.4 mmol) to provide after purification by silica-gel flash chromatography (silica-gel 15-40 μm, hexane/EtOAc, 9:1) 590 mg (37%) of the odoriferous title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08182781B2
Source datasetuspto-grants-2012_05
ORD IDord-50b243d8c94547a3a7674b8337205258
Source noteuspto-grants-2012_05