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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584213Generated: October 29, 2026

Dimethylformamide → 4-(Tert-butyldiphenylsilyloxymethyl)-3-methylbenzaldehyde

https://huagongshe.com/reaction/584213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Bromo-4-(tert-butyldiphenylsilyloxymethyl)-3-methylbenzeneHCID 22342689—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-(Tert-butyldiphenylsilyloxymethyl)-3-methylbenzaldehydeHCID 22342923—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 1-bromo-4-(tert-butyldiphenylsilyloxymethyl)-3-methylbenzene (2.19 g) in tetrahydrofuran (30 ml) was added 1.6 M butyllithium in hexane (4.69 ml) by syringe under nitrogen atmosphere at −78° C. After 30 minutes of stirring at −78° C., N,N-dimethylformamide (1.16 ml) was added to the solution at −78° C. and then the mixture was allowed to warm to 5° C. over 1.5 hours. Saturated ammonium chloride solution (10 ml) was added to the mixture and the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The combined extract was washed with water, dried over magnesium sulfate, and concentrated under reduced pressure to give 4-(tert-butyldiphenylsilyloxymethyl)-3-methylbenzaldehyde (1.90 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924278B2
Source datasetuspto-grants-2005_08
ORD IDord-dbd503d70030487b83e01f727d4a039e
Source noteuspto-grants-2005_08