HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963272Generated: October 30, 2026
Imidazole → (7S,10R)-2-(tert-Butyldimethylsiloxy)-7,8,9,10-tetrahydro-9,9-dimethoxy-7-methyl-10-phenanthridinol
https://huagongshe.com/reaction/963272
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | (7S,10R)-7,8,9,10-Tetrahydro-9,9-dimethoxy-7-methyl-2,10-phenanthridinediol | HCID 57292997 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (7S,10R)-2-(tert-Butyldimethylsiloxy)-7,8,9,10-tetrahydro-9,9-dimethoxy-7-methyl-10-phenanthridinol | HCID 11101514 | 91.4% |
Reaction Steps
Imidazole (1.01 g, 14.8 mmol, 2.60 equiv) and t-butyldimethylsilyl chloride (1.11 g, 7.39 mmol, 1.30 equiv) were added sequentially to a solution of (7S,10R)-7,8,9,10-tetrahydro-9,9-dimethoxy-7-methyl-2,10-phenanthridinediol (16, 1.64 g, 5.69 mmol, 1 equiv) in N,N-dimethylformamide (10 mL) at 23° C. After stirring for 1 h at 23° C., the reaction mixture was partitioned between water (100 mL) and ethyl acetate (100 mL). The aqueous layer was separated and extracted further with two 100-mL portions of ethyl acetate. The combined organic layers were dried over sodium sulfate and were concentrated. The residue was purified by flash column chromatography (30% ethyl acetate-hexanes) to afford (7S,10R)-2-(tert-butyldimethylsiloxy)-7,8,9,10-tetrahydro-9,9-dimethoxy-7-methyl-10-phenanthridinol (17) as a light yellow foam (2.10 g, 91%). ##STR27##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763451 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-e0ec7caae5464254b67f951ef467cfff |
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| Source note | uspto-grants-1998_06 |
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