HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629695Generated: October 27, 2026
Dimethyl Sulfoxide → Tert-butyl (2S,5S)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-formylmorpholine-4-carboxylate
https://huagongshe.com/reaction/629695
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Tert-butyl (2S,5S)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-(hydroxymethyl)morpholine-4-carboxylate | HCID 86726301 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl (2S,5S)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-formylmorpholine-4-carboxylate | HCID 86726303 | — |
Reaction Steps
To a stirred solution of oxalyl chloride (2 eq) in DCM (0.3 M) at −78° C. was added a solution of DMSO (5 eq) in DCM (0.5M). The reaction mixture was stirred at −78° C. for 30 min. A solution of tert-butyl (2S,5S)-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-(hydroxymethyl)morpholine-4-carboxylate (1 eq) in CH2Cl2 (0.2M) was added dropwise and stirred at −40° C. for 1.5 hours. It was then cooled to −78° C. and triethylamine (7 eq) was added and the reaction mixture was stirred at 0° C. for 1 h. Water was added and the reaction mixture was warmed to rt for 30 min. The mixture was diluted with CH2Cl2, the organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated. The crude product was used as such for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315475B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-4eb63425462545c59f4669ca39e92ca9 |
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| Source note | uspto-grants-2016_04 |
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