HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613430Generated: October 31, 2026
Hydrochloric Acid → HCID 178500464, compound
https://huagongshe.com/reaction/613430
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nsc 634137 | HCID 184894 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 178507164 | HCID 178507164 | — |
| Reactant | HCID 178519241 | HCID 178519241 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178500464 | HCID 178500464 | 19% |
Reaction Steps
A solution of bis(2,2,2-trifluoroethyl)(methoxycarbonylmethyl)phosphonate (0.648 g, 2.04 mmol, 1.2 eq) and 18 crown 6 (2.24 g, 8.5 mmol, 5.0 eq) in tetrahydrofuran (30 mL), was cooled to n78° C. To this at n78° C. was added potassium bis(trimethylsilyl)amide (4.08 mL, 2.04 mmol, 1.2 eq). The reaction mixture was stirred at n78° C. for 30 min and treated with a solution of 2-imidazole-4-ylcyclopropanecarbaldehyde (0.64 g, 1.7 mmol) in tetrahydrofuran (5 mL). The reaction mixture was again stirred at n78° C. for 1 hour, treated with aqueous satd. ammonium chloride solution and extracted with ether. The organic layer was separated, washed with water and dried over anhyd. Na2SO4. Crude product was purified by flash column eluted with ethyl acetate: hexane (1:3) to give trityl protected product (0.730 g). A small amount (150 mg) of this product was deprotected by treatment with 2 N HCl at 90° C. for 1 h to give final product (yield=62 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06008240 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-b9b8b4627f744e68911fca101c14932b |
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| Source note | uspto-grants-1999_12 |
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