HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175146Generated: November 2, 2026
Hydrochloric Acid → 4-(2-Morpholin-4-yl-ethoxy)-benzamidine
https://huagongshe.com/reaction/1175146
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-(2-Morpholin-4-ylethoxy)benzonitrile | HCID 2994074 | — |
| Reactant | HCID 178418261 | HCID 178418261 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-Morpholin-4-yl-ethoxy)-benzamidine | HCID 28394944 | 93% |
Reaction Steps
4-(2-Morpholin-4-yl-ethoxy)-benzonitrile (Maybridge CC 42116)(2.7 g; 11.64 mmol) in THF (10 ml) is combined with LiN(TMS)2 (30 mmol; 30 ml of a 1M solution in THF) and stirred for 30 minutes at 55° C., kept at room temperature for 30 minutes and cooled to 5° C., while 3N HCl (28 ml) is added slowly. After 10 minutes the reaction mixture is washed with TBME and the aqueous phase is adjusted to pH ˜11 with solid NaOH, saturated with solid K2CO3 and extracted with TBME/MeOH (˜10:1) several times. The combined organic phases are dried over Na2SO4, filtered and evaporated to yield the title compound as yellow crystals (2.7 g; 93%). 1H-NMR (400 MHz; DMSO-d6): 7.72 (d, 2H); 6.96 (d, 2H); 6.31 (bs, 3H); 4.13 (t, 2H); 3.59 (m, 4H); 2.71 t, 2H); 2.49 (m, 4H). MS (m/z) ES+: 250 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07838674B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-3601e3956bd24c9eb731d21860811e33 |
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| Source note | uspto-grants-2010_11 |
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