HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358256Generated: November 3, 2026
Hydrochloric Acid → HCID 136355272, compound
https://huagongshe.com/reaction/2358256
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | HCID 53434041 | HCID 53434041 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136355272 | HCID 136355272 | — |
Reaction Steps
To a solution of the intermediate from Example 1 Step A (48 g, 0.163 mol) in ethanol (800 mL) at −10° C. was added dropwise t-butylnitrite (22.1 mL, 0.18 mol) over 10 minutes, followed by 2.5 N HCl in absolute ethanol (52 mL, 0.13 mol). The reaction temperature was maintained at −5° C. during these additions. After the addition was completed, the dry ice bath was removed and the reaction was allowed to warm to RT overnight. The ethanol was removed under reduced pressure and the residue was diluted with H2O. The aqueous phase was made basic with saturated NaHCO3 and extracted with EtOAc. The combined organic extracts were washed with brine, dried over Na2SO4 and concentrated under reduced pressure. The crude residue was taken up in methanol/isopropanol and mixed with toluene. The methanol/isopropanol mixture was concentrated under reduced pressure and the title compound was recrystallized from hexane/toluene. 1H NMR (400 MHz, CDCl3): δ8.22 (m, 1H), 7.78 (m, 2H), 7.65 (m, 2H), 7.32 (m, 1H), 7.08(s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07763634B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-f3ef9ac1e6784bd8918072954ae38946 |
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| Source note | uspto-grants-2010_07 |
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