HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768464Generated: October 30, 2026
HCID 23614737, compound → HCID 10406948, compound
https://huagongshe.com/reaction/1768464
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 23614737 | HCID 23614737 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10406948 | HCID 10406948 | — |
Reaction Steps
To a suspension of 75 mg (0.21 mmol) of aldehyde 3-1 in THF at −78° C. was added 80 μL (0.25 mmol) of methyl magnesium bromide solution (3M in Et2O). After stirring 1 h at that temperature, an additional 80 μL of the Grignard reagent was added and stirring was continued for 1 h more. The reaction was quenched with saturated NH4Cl, partitioned between brine and EtOAc, the organic phase washed with brine, dried over MgSO4, and concentrated. The residue was purified by column chromatography on silica gel with EtOAc/hexanes to provide 5-1 as a white solid. Data for 5-1: 1HNMR (500 MHz, CDCl3) δ 7.6 (m, 2H), 7.4-7.2 (m, 3H), 7.1-6.9 (m, 3H), 6.5 (s, 1H), 5.05 (m, 1H), 4.8 (m, 1H), 4.6 (m, 1H), 4.35 (m, 1H), 2.8 (s, 6H), 1.4 (m, 3H) ppm. HRMS (ES) calc'd M+H for C21H22F2N2O2: 373.1722. Found: 373.1713.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235580B2 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-35c7891300c64750b5791d19ef4bc0fd |
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| Source note | uspto-grants-2007_06 |
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