HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416002Generated: October 26, 2026
Sodium borohydride → 2-benzyloxymethyl-5-(3,5-dichlorophenylthio)-1-(2-hydroxypropyl)-4-isopropyl-1H-imidazole
https://huagongshe.com/reaction/1416002
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-acetylmethyl-5-(3,5-dichlorophenylthio)-4-isopropyl-2-(p-methoxybenzyloxymethyl)-1H-imidazole | HCID 22130987 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-benzyloxymethyl-5-(3,5-dichlorophenylthio)-1-(2-hydroxypropyl)-4-isopropyl-1H-imidazole | HCID 22130353 | — |
Reaction Steps
In methanol (5 ml)was dissolved 371 mg (0.8 mmol)of 1-acetylmethyl-2-benzyloxymethyl-5-(3,5-dichlorophenylthio)-4-isopropyl-1H-imidazole (17v"), followed by addition of 38 mg (1.0 mmol)of sodium borohydride with stirring at room temperature, and the mixture was stirred for 1.5 hours. This reaction mixture was concentrated under reduced pressure, and to the residue were added water and methylene chloride to extract. The organic layer was washed with water and was dried over sodium sulfate. The solvent was concentrated under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate:methylene chloride=1:9), to obtain 2-benzyloxymethyl-5-(3,5-dichlorophenylthio)-1-(2-hydroxypropyl)-4-isopropyl-1H-imidazole (17v'")as oil quantitatively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05910506 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-2a1172edf800400e856b9db2f97f3d3f |
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| Source note | uspto-grants-1999_06 |
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