HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245798Generated: November 2, 2026
Hydroxylamine → 6-(4'-Chloro-biphenyl-4-sulfinyl)-hexanoic acid hydroxyamide
https://huagongshe.com/reaction/2245798
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 6-(4'-Chloro-biphenyl-4-ylsulfinyl)-hexanoic acid methyl ester | HCID 10067377 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-(4'-Chloro-biphenyl-4-sulfinyl)-hexanoic acid hydroxyamide | HCID 10316799 | 79% |
Reaction Steps
To a solution of the 6-(4′-chloro-biphenyl-4sulfinyl)-hexanoic acid methyl ester (400 mg, 1.1 mmol) in distilled THF (10 mL) containing 50% aqueous hydroxylamine (0.65 mL, 9.9 mmol) was added at 0° C. a solution of potassium hydroxide in methanol (1.9 mL, 1M, 1.9 mmol) in a dropwise manner. After stirring at 0° C. for 1 h, distilled water (10 mL) was added and the mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C. The aqueous solution was extracted with ethyl acetate (2×20 mL) and the combined extracts were washed with brine (40 mL), dried over anhydrous MgSO4, filtered and evaporated to dryness. The residue was recrystallised from acetone to give the title compound (315 mg, 79%) as a white powder, mp 108-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07683185B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-27d2117e8c0143989482d4f595f770cf |
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| Source note | uspto-grants-2010_03 |
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