HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585565Generated: October 26, 2026
Acetic Acid → 5-tert-butoxy-5-oxo-3-[(phenylthio)methyl]pentanoic Acid
https://huagongshe.com/reaction/585565
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Tert-butyl (5-oxotetrahydrofuran-3-yl)acetate | HCID 13641874 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-tert-butoxy-5-oxo-3-[(phenylthio)methyl]pentanoic Acid | HCID 21927879 | 35% |
Reaction Steps
The product from step 1 (200 mg, 1.0 mmoles) and thio phenol (110 mg, 1 mmoles) were combined in dimethyl formamide (1.5 mL) at room temperature. Lithium(bis trimethyl silyl)amide (1.25 mL of a 1M solution in THF) was added and the reaction heated at 80° C. for 18 h. Reaction was diluted with water, made acidic with acetic acid and extracted with dichloromethane 2×40 mL. The combined extracts were washed with water 2×50 mL, brine 1×50 mL, dried and the solvent removed under pressure. The crude was chromatographed to give the product 108 mg (35%). MS (ESI+) for C16H22O4S m/z 333 (M+Na)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06933304B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-fd51bf03358a4295b5a636fa13f435d4 |
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| Source note | uspto-grants-2005_08 |
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