HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444577Generated: October 25, 2026
Dimethyl Sulfoxide → (S)-2-Boc-aminobutyraldehyde
https://huagongshe.com/reaction/1444577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Monosodium phosphate | HCID 23672064 | — |
| Reactant | 2(S)-Boc-aminobutanol | HCID 86602354 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-2-Boc-aminobutyraldehyde | HCID 86590935 | 90.7% |
Reaction Steps
A solution of oxalyl chloride (40.39 g, 265 mmol) in MeCl2 (700 mL) was stirred and cooled to −60° C. Dimethylsulfoxide (51.7 g, 663 mmol) in MeCl2 (100 mL) was added dropwise. After 10 min., a solution of 2(S)-Boc-amino-1-butanol (50 g, 265 mmol) in MeCl2 (100 mL) was added dropwise at −70° C. The reaction mixture was allowed to warm to −40° C. for 10 min. and then cooled to −70° C. again. A solution of triethylamine (74.9 g, 742 mmol) in MeCl2 (100 mL) was added. The reaction mixture was allowed to warm to room temperature over 2 h. Saturated sodium dihydrogen phosphate (100 mL) was added, and then the organic layer was washed with brine and dried over MgSO4. The solvent was removed to yield 45 g of 2(S)-Boc-aminobutyraldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662849B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-22262693cce1482a882c65b1e77b50b8 |
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| Source note | uspto-grants-2010_02 |
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