Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Tert-butylcyclopentadiene | HCID 633714 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 86662536 | HCID 86662536 | — |
Reaction Steps
In a 1000 ml five neck flask, 24.97 g (204 mmol) of tert-butylcyclopentadiene and 399.04 g of acetone were placed. In an ice water bath, 82.1 g (1.15 mol) of pyrolydine was dropwise added, followed by stirring for 18 hours under reflux. In an ice water bath, 70.91 g (1.18 mol) of acetic acid was dropwise added. From the resulting crude product, the solvent was distilled off under reduced pressure (150 torr, 40° C.), and the resulting product was washed with water, a 5% acetic acid solution, a saturated sodium hydrogen carbonate aqueous solution and a saturated saline solution, followed by drying over magnesium sulfate. After the solvent was distilled off, the remainder was purified by vacuum distillation, whereby 23.4 g of 5-tert-butyl-1,1,3-trimethyl-1,2-dihydropentalene represented by the following formula [1] was obtained. Identification was carried out by a 1H-NMR spectrum and a GC-mass spectrometry spectrum (GC-MS). The results of the measurement are given below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08409480B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-2d9c972faa7a4c6a99be7accac8a28c4 |
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| Source note | uspto-grants-2013_04 |
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