Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2255547Generated: November 1, 2026

Acetic Acid → HCID 178441506, compound

https://huagongshe.com/reaction/2255547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 131718096HCID 131718096—
CatalystHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
ProductHCID 178441506HCID 17844150665%

Reaction Steps

To a solution of 0.073 g (0.099 mmol) of the product from Example 42 in 2 mL of MeOH was added 4 drops of conc. HCl. The reaction mixture was stirred for 5 minutes and then made basic by addition of conc. NH4OH. The pH of the solution was adjusted to 5.0 by addition of acetic acid. The reaction mixture was concentrated in vacuo and the residue was taken up in 20 ml of EtOAc. The solution was washed with water (2×5 mL) and brine (1×5 mL) and dried over MgSO4. The mixture was filtered and concentrated in vacuo. The crude product was very insoluble and was consequently purified by trituration with CHCl3, EtOAc and hexanes to give 32 mg of an off white solid, 65% yield. 1H-NMR (CD3OD 300 MHz): 0.83 (t, 3H, J=7.3 Hz), 1.32 (m, 2H), 1.62 (2H, m), 2.09 (s, 2H), 2.68 (3 line m, 2H, J=8.1 Hz), 5.37 (bs, 2H), 7.00-7.10 (m, 4H), 7.42-7.61 (m, 5H), 7.89 (dd, 1H, J=2.4, 8.8 Hz), 8.39 (d, J=2.5 Hz). FABMS m/e: 494(M+ +1) calc. for C28H27N7O2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05240928
Source datasetuspto-grants-1993_08
ORD IDord-e7013da56d504e58ad7f26bd0842c990
Source noteuspto-grants-1993_08