Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 6-Bromohexanoyl chloride | HCID 89848 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10944045 | HCID 10944045 | 90% |
Reaction Steps
A solution of 27.5 g (0.610 mole) of dimethylamine in 100 ml of cold tetrahydrofuran was added dropwise to a solution of 25.0 g (0.117 mole) of 6-bromohexanoyl chloride in 100 ml of tetrahydrofuran. The reaction mixture was stirred mechanically and the temperature maintained between 5° and 15° C. throughout the addition. After the final addition, the solution was filtered to remove the solid precipitate and the filtrate was concentrated under reduced pressure to yield 23.3 g (90%) of light-yellow oil. An analytical sample was prepared by filtering the oil through a small bed of silica gel and eluting with ethyl acetate. The fractions containing the desired product were combined and concentrated under reduced pressure to give the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05057524 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-ded0816f7d2b41af8d7f84b3ce32cff0 |
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| Source note | uspto-grants-1991_10 |
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