HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172825Generated: October 25, 2026
Hexane → [4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanol
https://huagongshe.com/reaction/1172825
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hexane | HCID 8058 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (2-Chloro-6-fluoro-3-methoxyphenyl)trimethylsilane | HCID 46941339 | — |
| Reactant | 4-(4-Chlorophenoxy)-2-propylbenzaldehyde | HCID 57420143 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | [4-Chloro-2-fluoro-5-methoxy-3-(trimethylsilyl)phenyl][4-(4-chlorophenoxy)-2-propylphenyl]methanol | HCID 86622409 | — |
Reaction Steps
To a solution of 2,2,6,6-tetramethylpiperidine (2.75 g, 10 mmol) in THF (50 mL) cooled at −75° C. was added a solution of n-butyllithium in hexane (1.6 M, 6.3 mL, 10 mmol). After 15 min, 4-fluoro-2-chloro-3-(trimethylsilyl)anisole (2.3 g, 10 mmol) was added and the solution was warmed gradually to −40° C. over a 2 h period. The solution was recooled to −75° C. and a solution of the aldehyde from Step 1 of Example 3 (1.4 g, 5.0 mmol) in THF (3 mL) was added quickly. The reaction mixture was stirred for 15 min., poured into a saturated aqueous solution of ammonium chloride and extracted with ethyl acetate. After removal of the solvent, the residue was purified by chromatography on silica gel to give the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834036B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-8ab7dbe4dfac470a9b7aa4d9fdbe6be1 |
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| Source note | uspto-grants-2010_11 |
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