HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367243Generated: October 30, 2026
Diethyl Ether → Methyl (5S)-5-[(tert-butylsulfinyl)amino]-5-(3,5-difluorophenyl)-2,2-dimethylhexanoate
https://huagongshe.com/reaction/1367243
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | methyl (5E)-5-tert-butylsulfinylimino-5-(3,5-difluorophenyl)-2,2-dimethylpentanoate | HCID 87221342 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl (5S)-5-[(tert-butylsulfinyl)amino]-5-(3,5-difluorophenyl)-2,2-dimethylhexanoate | HCID 66973479 | — |
Reaction Steps
To a solution of methyl (5E)-5-[(tert-butylsulfinyl)imino]-5-(3,5-difluorophenyl)-2,2-dimethylpentanoate (342 mg, 0.920 mmol) in CH2Cl2 (6 mL) at 0° C., was added dropwise over five minutes methyl magnesium bromide as a 3M solution in diethyl ether (0.61 mL, 1.83 mmol). After 15 minutes the reaction was determined to be complete by LCMS analysis. The reaction was quenched by the dropwise addition of 1M HCl (5 mL), followed by 5 mL of water. The aqueous layer was extracted once with CH2Cl2 (10 mL) and the organics were combined and washed once with brine (15 mL). The organics were dried over sodium sulfate, filtered and concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of EtOAc:Hexanes—10:90 to 55:45, to give the title compound. MS: m/z=390 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893079B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-0af6bbd7ef3642aba49faa04ab135960 |
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| Source note | uspto-grants-2011_02 |
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