Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | β-Hydromuconic acid diethyl ester | HCID 6148048 | — |
| Product | HCID 70048597 | HCID 70048597 | 71% |
Reaction Steps
To a stirred solution 688 mg (3.44 mmol) trans-2-butene-1,4-dicarboxylic acid diethyl ester in 35 ml THF was added 1.46 g (34.4 mmol) anhydrous lithium chloride and the resulting suspension cooled to −78° C. 3.44 ml (6.88 mmol) of a 2 M solution of LDA in THF was added dropwise and stirring continued for 45 min. 0.82 ml (6.9 mmol) benzyl bromide was then added and stirring continued for 1 h at −78° C. and 10 min at 0° C. The reaction was quenched at this temperature by addition of saturated ammonium chloride solution and the mixture extracted three times with ether. The combined organic phases were washed with saturated brine, dried over sodium sulphate, and concentrated in vacuo. Flash chromatography (5% EtOAc in hexane) afforded 927 mg (71%) of the title compound as a yellow oil. MS m/e (%): 398 ([M+NH4]+, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06262089B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-83229691c63048b1958bbbf1fbb0e27b |
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| Source note | uspto-grants-2001_07 |
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