Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Tert-butyl 2,2,2-trichloroethanimidate | HCID 2734700 | — |
| Reactant | HCID 21197492 | HCID 21197492 | — |
| Catalyst | Boron trifluoride etherate | HCID 8000 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | HCID 17932014 | HCID 17932014 | 79.1% |
Reaction Steps
To a solution of α-bromoglutaric acid-5-benzylester (See Example 18a(i)(a); 1.2 g, 4.0 mmol) in chloroform (Merck, 5 mL) a solution of tert-butyl 2,2,2-trichloroacetimidate (Fluka, 1.57 mL, 8.52 mmol) in cyclohexane (Merck, 5 mL) was added dropwise over 5 minutes. N,N-Dimethylacetamide (Fluka, 0.88 mL) was added followed by boron trifluoride ethyl etherate (Aldrich, 80 μL) as catalyst. The reaction mixture was stirred for 5 days at room temperature. Hexane was added and the organic phase washed with brine three times, dried over sodium sulphate and evaporated under reduced pressure. The crude product was purified using normal phase chromatography (Silica column (40 g), solvents: A=hexane, B=ethyl acetate, gradient: 10 to 35% B over 15 min, flow rate 40 mL/min, UV detection at 214 and 254 nm) affording 1.13 g (79%) of the pure product. Structure was verified by NMR
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09061080B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-05082266f0714dfaa634dbb968f0fe93 |
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| Source note | uspto-grants-2015_06 |
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