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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613430Generated: October 31, 2026

Hydrochloric Acid → HCID 178500464, compound

https://huagongshe.com/reaction/613430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantNsc 634137HCID 184894—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantHCID 178507164HCID 178507164—
ReactantHCID 178519241HCID 178519241—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178500464HCID 17850046419%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008240
Source datasetuspto-grants-1999_12
ORD IDord-b9b8b4627f744e68911fca101c14932b
Source noteuspto-grants-1999_12