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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N-bis(trimethylsilyl)-3-bromo-1-propylamine | HCID 11044237 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67079576 | HCID 67079576 | 76% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07906592B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-fa3804908a0e420586846297aaacb612 |
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| Source note | uspto-grants-2011_03 |
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