HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966978Generated: November 1, 2026
Ammonium Chloride → HCID 22293462, compound
https://huagongshe.com/reaction/966978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 8-Phenyl-1,4-dioxaspiro[4.5]decane-8-carbaldehyde | HCID 12230275 | — |
| Reactant | HCID 22293456 | HCID 22293456 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22293462 | HCID 22293462 | 92% |
Reaction Steps
Lithium hexamethyldisilazide (1M in tetrahydrofuran, 7.0 mL, 7.0 mmol) was added over 10 minutes to a cooled (−78° C.) solution of 8-phenyl-1,4-dioxaspiro[4,5]decane-8-carboxaldehyde (J. Med. Chem. 1975, 18, 593-599, 1.68 g, 6.8 mmol) and 2-({(2-[3,5-bis(trifluoromethyl)phenyl]ethyl}sulfonyl)benzothiazole (Description 34, 2.99 g, 6.8 mmol) in tetrahydrofuran (15 mL) and the mixture was stirred at −78° C. for 1 hour, then allowed to warm to room temperature. Aqueous ammonium chloride (saturated, 10 mL) was added and the mixture was stirred at room temperature for 30 minutes. Water (5 mL) was added and the mixture was extracted with ethyl acetate (3×30 mL). The combined organic fractions were washed with brine (50 mL), dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with isohexane/EtOAc (90:10) to give the tide compound as a pale yellow oil (2.43 g, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953792B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-323412f03ef34f87bfe12838cf0ad47a |
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| Source note | uspto-grants-2005_10 |
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