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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279370Generated: October 31, 2026

Acetic Acid → HCID 86755984, compound

https://huagongshe.com/reaction/279370

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantButanalHCID 261—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86755985HCID 86755985—
SolventWaterHCID 962—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 86755984HCID 8675598484.9%

Reaction Steps

A solution of cis-(3,5-bis-trifluoromethyl-benzyl)-(6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydro-quinolin-4-yl)-carbamic acid methyl ester (Example 67) (34 mg, 0.067 mmol), acetic acid (4 μL, 0.067 mmol), butyraldehyde (17 μL, 0.34 mmol), and sodium triacetoxyborohydride (71 μL, 0.34 mmol) in anhydrous dichloroethane (1 mL) were stirred at room temperature overnight. Water (5 mL) was added, the aqueous phase made basic with potassium carbonate, and the mixture was extracted with ethyl acetate (3×10 mL). The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. Purification by silica gel chromatography using 0-15% ethyl acetate/hexanes as eluent afforded 32 mg of the title compound (82%): MS m/z 563 (M++1); 1H NMR (CDCl3) δ6.31 (C8, s, 1H), 3.64 (CO2Me, s, 3H), 1.20 (C2-Me, d, 3H, J=6.3 Hz). The hydrochloride salt was prepared by treating an ethereal solution of the free base with an ethereal solution of HCl. Hydrochloride salt: 1H NMR (CDCl3) δ3.83 (CO2Me, s, 3H), 1.20 (C2-Me, d, 3H, J=6.4 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362198B1
Source datasetuspto-grants-2002_03
ORD IDord-440658382b874ac7ad15fa9f035b124e
Source noteuspto-grants-2002_03