HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425796Generated: October 30, 2026
Dimethyl Sulfoxide → (1S,2S,5R)-2-formyl-7-methyl-3-aza-bicyclo[3.3.0]-octane-3-carboxylic acid tert.-butyl ester
https://huagongshe.com/reaction/425796
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (1S,2S,5R)-2-hydroxymethyl-7-methyl-3-aza-bicyclo[3.3.0]-octane-3-carboxylic acid tert.-butyl ester | HCID 66703846 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (1S,2S,5R)-2-formyl-7-methyl-3-aza-bicyclo[3.3.0]-octane-3-carboxylic acid tert.-butyl ester | HCID 86643542 | — |
Reaction Steps
To a cold (−60° C.) solution of oxalyl chloride (0.081 mL, 1.2 eq) in dry DCM (2.2 mL) was added dropwise a solution of DMSO (0.13 mL, 2.2 eq) in dry DCM (1.7 mL) within 4 min. After 10 min, was added dropwise (1S,2S,5R)-2-hydroxymethyl-7-methyl-3-aza-bicyclo[3.3.0]-octane-3-carboxylic acid tert.-butyl ester (206 mg) in dry DCM (1.2 mL) during 5 min. After 2 min a white suspension was formed. Stirring was continued 30 min at −55° C., then DIPEA (0.690 mL, 5 eq) (which was dried over 3A M.S.) was added during 3-4 min. The reaction mixture was allowed to come to RT, diluted with water and extracted with DCM. The combined org. extracts were washed with citric acid (5%), brine, dried over anh. MgSO4, filtered and evaporated to yield the title compound as an oil, which was used for the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106215B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-90a6390a916b42539bec1d8bbd43bad4 |
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| Source note | uspto-grants-2012_01 |
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