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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1991523Generated: November 1, 2026

Hydrochloric Acid → HCID 68539250, compound

https://huagongshe.com/reaction/1991523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58909344HCID 58909344—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 68539250HCID 68539250—

Reaction Steps

To 1.98 g (3.8 mmol) of compound 5 in 15 mL of CH2Cl2 is added 6.5 mL of trifluoroacetic acid. The mixture is stirred under a nitrogen atmosphere for 1 h and then concentrated. The resulting residue is taken up in ethyl acetate and washed twice with 10% Na2CO3 and once with 1 N NaHCO3. The organic layer is dried over anhydrous Na2SO4, filtered, and concentrated to afford 1.6 g (quant.) of a pale yellow oil (free base of 6), which is generally carried on in the next step without characterization. The yellow oil may be dissolved in ether and treated with ethereal HCl to precipitate (dihydrochloride 6 as a white solid after trituration with ether: 1H NMR (CDCl3+CD3OD drop) δ 7.55 (s, 1H), 7.45-7.15 (m, 3H), 6.85 (m, 2H), 6.75 (m, 1H), 4.4 (d, J=9.5 Hz, 1H), 3.82 (m, 1H), 2.97 (m, 2H), 2.81 (dd, J=8, 14 Hz, 1H), 2.65 (m, 2H), 2.5 (obscured by water) 2.26 (m, 1H), 2.13 (m, 2H), 1.79 (m, 2H), 1.59 (m, 1H), 1.45-1.25 (m, 3H), 1.28 (d, J=7 Hz, 6H); MS (CI) m/z 417.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645780B2
Source datasetuspto-grants-2010_01
ORD IDord-b2e9e34ae38b4db78bdbf728e849a156
Source noteuspto-grants-2010_01