HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413369Generated: November 2, 2026
Boron trifluoride → 2-(4-Ethylbenzoyl)benzoic acid
https://huagongshe.com/reaction/2413369
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | HCID 54297901 | HCID 54297901 | — |
| Product | 2-(4-Ethylbenzoyl)benzoic acid | HCID 70852 | — |
Reaction Steps
A complex of ortho-(4-ethylbenzoyl)benzoic acid (OEBB acid) is prepared according to U.S. Pat. No. 4,379,092 by reacting 26.6 g phthalic anhydride, 19.07 g ethylbenzyne, 35.9 g HF, and 121.77 g BF3 for 30 minutes at -40° C. After reaction and degassing at -40° C., 144.4 g of a complex solution in HF is obtained. This solution is injected over a 20 minute period into the column described in Example 1. The same temperature and pressure conditions were used and methylene chloride was again selected as the solvent. The methylene chloride reflux rate was 3.8 kg/h. After introducing the complex solution, the solvent reflux was maintained for 20 minutes before evaporating the solvent in the boiler. 43.31 g of crude OEBB acid which contained 39.07 g of OEBB acid was recovered. Also, the recovery rates for BF3 and HF were 99.3% and 99.6%, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04496760 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-6d5908596e1d4281996e380a4430febc |
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| Source note | uspto-grants-1985_01 |
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