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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785615Generated: October 31, 2026

Hydrochloric Acid → HCID 68427487, compound

https://huagongshe.com/reaction/1785615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
ReactantHCID 68425957HCID 68425957—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68427487HCID 68427487104.7%

Reaction Steps

A solution of 2-(R)-(4-methoxyphenyl)-2-[2-(4-methoxyphenyl)-acetylamino]-acetamide (316 g, 0.96 mol) in THF (2 L) is heated to 35° C. and borane dimethyl sulfide (428 mL, 4.28 mol) is added over approximately 1 hour after which the reaction is heated to reflux for 18 hours. After cooling the reaction solution to 8° C. sufficient 3N HCl (approx. 400 mL) is added until the pH of the solution is approximately 1. The reaction solution is then heated to reflux for 1 hour. The reaction is then cooled and the pH adjusted to 8 by the slow addition of 25% aqueous NaOH (300 mL). The entire reaction solution is poured into a vessel containing a mixture of CH2Cl2 (3 L) and water (1.5 L). The organic layer is decanted and the water layer treated with CH2Cl2 (1.5 L). The organic layers are combined, washed with brine (2.5 L) then dried over Na2SO4. The solvent in removed in vacuo to afford 302 g (quantitative yield) of the desired product as an amber colored oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504517B2
Source datasetuspto-grants-2009_03
ORD IDord-efd2d005c4974fceb69e34e9a02f044a
Source noteuspto-grants-2009_03