Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Reactant | HCID 178420676 | HCID 178420676 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 68719156 | HCID 68719156 | 88.7% |
Reaction Steps
Under nitrogen atmosphere, 1300 mL (2.60 mol, 1.00 eq) of 2.0M methylmagnesium chloride-tetrahydrofuran solution was cooled, and 322.7 g (2.60 mol, 1.00 eq) of 2-fluorobenzaldehyde was added while adjusting the inside temperature to −20 to +2° C., followed by stirring for 30 minutes under a cooled condition in iced water. Conversion of methylation was 99.9% by determination by gas chromatography. Subsequently, while adjusting the inside temperature to −22 to 0° C., 385.1 g (2.60 mol, 1.00 eq) of phthalic anhydride was added, followed by stirring at room temperature through the night. Conversion of acylation was 99% or greater by determination by 1H-NMR. 1300 mL (2.60 mol, 1.00 eq) of 2.0N hydrochloric acid was added to the reaction-terminated liquid, followed by extraction with 650 mL of toluene. The recovered organic layer was washed with 650 mL of brine, dried with anhydrous sodium sulfate, concentrated under reduced pressure, and vacuum dried, thereby obtaining 706.1 g of racemic 1-(2-fluorophenyl)ethyl alcohol phthalate half ester represented by the following formula,
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795478B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-7896cd91c7df42ce943d717f2b6f71d6 |
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| Source note | uspto-grants-2010_09 |
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