HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724176Generated: October 29, 2026
Sodium sulfate decahydrate → HCID 11751892, compound
https://huagongshe.com/reaction/1724176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | HCID 11328654 | HCID 11328654 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11751892 | HCID 11751892 | — |
Reaction Steps
To a solution of 230 mg (0.5 mmol) of 1-{1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-1-(3,5-difluorophenyl)acetone in 10 mL of THF was added slowly a solution of 0.42 mL (1.25 mmol) of methylmagnesium chloride (3.0M solution in THF) at −78° C. and stirred for 1 h. The reaction mixture was warmed to 0° C. for 1 h, followed by adding 1 g of sodium sulfate decahydrate to quench the reaction, and stirring for 1 h at rt. The quenched reaction mixture was filtered and the organic layer was dried over Na2SO4 and concentrated. The residue was purified by silica gel chromatography with hexanes/acetone=8:1 to afford racemic 1-{1-[bis(4-chlorophenyl)methyl]azetidin-3-yl}-1-(3,5-difluorophenyl)-2-methylpropan-2-ol as a white solid. The enantiomers were separated by a chiral column (OJ Column with hexanes/ethyl alcohol); 1H NMR(CDCl3) δ 1.06 (s, 3H), 1.15 (S, 3H), 2.29 (t, 1H, J=7.5 Hz), 6.73 (m, 3H), 7.21-7.33 (m, 8H); Mass Spectrum: m/e=476 (M+1 35Cl, 35Cl) and 478 (M+1 35Cl, 37Cl).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07485732B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-ac5b050b3c3843539894b8bdb4b89142 |
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| Source note | uspto-grants-2009_02 |
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