HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904819Generated: October 26, 2026
O-Phenylenediamine → 2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazole
https://huagongshe.com/reaction/1904819
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(1-Benzylpiperidin-4-yl)acetic acid hydrochloride | HCID 14012844 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[[1-(phenylmethyl)-4-piperidinyl]methyl]-1H-benzimidazole | HCID 14012845 | — |
Reaction Steps
To 73 parts of hot (70° C.) polyphosphoric acid were added 27 parts of 1-(phenylmethyl)-4-piperidineacetic acid hydrochloride: temperature rose to 100° C. When the addition was complete, there were added portionwise 14 parts of 1,2-benzenediamine and stirring and heating was continued for 50 minutes at 170° C. The hot reaction mixture was poured into 300 parts of warm water. The acid solution was alkalized with a potassium hydroxide solution. The precipitated free base was filtered off, washed with water and extracted with trichloromethane. The extract was dried and evaporated. The solid residue was recrystallized from a mixture of 2-propanone and methanol, yielding 17 parts of 2-[[1-(phenylmethyl)-4-piperidinyl]-methyl]-1H-benzimidazole; mp. 221.5°-222° C. (compound 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04839374 |
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| Source dataset | uspto-grants-1989_06 |
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| ORD ID | ord-cd7c051a93894835a3416bb5c78bcfc8 |
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| Source note | uspto-grants-1989_06 |
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