Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741720Generated: October 31, 2026

Hydrochloric Acid → HCID 70084488, compound

https://huagongshe.com/reaction/741720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
ReactantAzidotrimethylsilaneHCID 78378—
Reactant5-(4-Cyanophenyl)pentanoic acidHCID 15280729—
Solvent1,2-DichloroethaneHCID 11—
SolventDimethylformamideHCID 6228—
ProductHCID 70084488HCID 70084488—

Reaction Steps

The product of step B (20.3 g, 0.10 mol) was dissolved in 1,2-dichloroethane (100 mL) and oxalyl chloride (62.5 g, 0.49 mol) was added, followed by DMF (50 μL). The solution was stirred at room temperature until gas evolution ceased (c.a. 30 min). The solvent and excess oxalyl chloride was removed under reduced pressure, redissolved in 200 mL of 1,2-dichloroethane and evaporated under reduced pressure again. The residue was dissolved in dry THF (150 mL) under nitrogen and azidotrimethylsilane (12.7 g, 0.11 mol) was added. After stirring at room temperature for 5 min., the stirred solution was heated in a 70° C. oil bath until gas evolution ceased (c.a. 1 hour). The solution was cooled in an ice bath and concentrated aq. HCl (20 mL) was added all at once and the ice bath was removed. After gas evolution ceased (c.a. 15 min) the solvent was removed under reduced pressure and the residue was partitioned between water and ethyl acetate. The aqueous layer was made basic (250 mL of 1N NaOH) and extracted with ethyl acetate. The organic layer was washed successively with water and sat'd. NaCl, dried (MgSO4), filtered and evaporated under pressure. The residue was redissolved in 150 mL of ethyl acetate and 20 mL of dry 6.9N HCl/dioxone was added with stirring and icebath cooling. The white precipitate was filtered and washed with ethyl acetate then diethyl ether affording 16.9 g (80%) of product: m.p. 155°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552431
Source datasetuspto-grants-1996_09
ORD IDord-70ffc97ca95544b0b79cda5c00fde749
Source noteuspto-grants-1996_09