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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602842Generated: October 31, 2026

N,N-bis(trimethylsilyl)-3-bromo-1-propylamine → HCID 67079576, compound

https://huagongshe.com/reaction/602842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-bis(trimethylsilyl)-3-bromo-1-propylamineHCID 11044237—
ReactantPhthalimide potassium saltHCID 24194345—
SolventDimethylformamideHCID 6228—
ProductHCID 67079576HCID 6707957676%

Reaction Conditions

Temperature80 °C

Reaction Steps

About 4.60 g of potassium phthalimide, 6.37 g of N,N-bis(trimethylsilyl)-3-bromo-1-propylamine, and 15 mL of N,N-dimethylformamide were mixed in a flask. The mixture was stirred for 6 hour while the flask was kept in an oil bath maintained at 80° C. The N,N-dimethylformamide was removed under vacuum. The residue was extracted with 90 mL of cyclohexane and filtered. The filtrate was evaporated under vacuum. The residue was triturated with 80 mL of hexane, cooled with dry ice, and then filtered to give N-[3-bis(trimethylsilyl)amino-1-propyl]phthalimide (BTMSAPPI) as a white solid (5.95 g, 76% yield). 1H NMR data (C6D6, 25° C., referenced to tetramethylsilane) of the product: δ 7.41 (multiplet, 2H, aromatic protons), 6.85 (multiplet, 2H, aromatic protons), 3.44 (triplet, J=7.1 Hz, 2H, CH2 protons), 2.81 (multiplet, 2H, CH2 protons), 1.75 (multiplet, 2H, CH2 protons), 0.06 (singlet, 18H, Si—CH3 protons).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906592B2
Source datasetuspto-grants-2011_03
ORD IDord-fa3804908a0e420586846297aaacb612
Source noteuspto-grants-2011_03