HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475192Generated: October 29, 2026
Dimethyl Sulfoxide → 1-(tetrahydro-2H-pyran-2-yl)-1H-benzo[d]imidazole-5-carbaldehyde
https://huagongshe.com/reaction/475192
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (1-(tetrahydro-2H-pyran-2-yl)-1H-benzo[d]imidazol-5-yl)methanol | HCID 58325018 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(tetrahydro-2H-pyran-2-yl)-1H-benzo[d]imidazole-5-carbaldehyde | HCID 86694723 | 72% |
Reaction Steps
To a solution of oxalyl chloride (1.17 g, 9.23 mol) in DCM (10 mL) at −70° C. was added dropwise DMSO (1.41 g, 18.09 mmol). The reaction mixture was stirred at −70° C. for 30 min. To the resulting solution was added dropwise over 30 min a solution of 24 (1.4 g, 6.03 mmol) in DCM (20 mL). After the addition the reaction temperature was raised to −55° C. The reaction was stirred for 1 h while the temperature was maintained between −55° C. and −45° C., then DIPEA (6.0 mL) was added dropwise over 5 min. The reaction mixture was warmed to 0° C. over 10 min then quenched with 1 M HCl (50 mL). The organic layer was separated, dried (MgSO4), filtered and concentrated in vacuo to afford 1.0 g (72%) of 1-(tetrahydro-2H-pyran-2-yl)-1H-benzo[d]imidazole-5-carbaldehyde (64) as red oil: MS (ESI) m/z=231.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08637537B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-ba20733ca1c448d8b33cf5ae47de6757 |
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| Source note | uspto-grants-2014_01 |
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