Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 67402090 | HCID 67402090 | — |
| Product | HCID 58418822 | HCID 58418822 | 76% |
Reaction Steps
A mixture of 3-(2-bromo-4-tert-butylphenyl)-2-methylpropanoic acid (46 g, 150 mmol) and SOCl2 (18 ml, 220 mmol) was stirred for 1 h at 40° C. The excess of SOCl2 was removed in vacuo. The residue was dissolved in CH2Cl2 (50 ml) and added at 0° C. to a suspension of 20 g AlCl3 in CH2Cl2 (200 ml). The reaction mixture was stirred overnight, poured into ice/water (500 g) containing 50 ml of conc. HCl. The organic phase was collected, washed with water, dried over MgSO4 and evaporated. The residue was distilled at 125-130° C. /0.5 torr giving 32 g (76%) of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858717B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-e20f596214bd41f3a5415403fd7a0b35 |
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| Source note | uspto-grants-2010_12 |
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