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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444577Generated: October 25, 2026

Dimethyl Sulfoxide → (S)-2-Boc-aminobutyraldehyde

https://huagongshe.com/reaction/1444577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMonosodium phosphateHCID 23672064—
Reactant2(S)-Boc-aminobutanolHCID 86602354—
SolventDichloromethaneHCID 6344—
Product(S)-2-Boc-aminobutyraldehydeHCID 8659093590.7%

Reaction Conditions

Temperature-60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662849B2
Source datasetuspto-grants-2010_02
ORD IDord-22262693cce1482a882c65b1e77b50b8
Source noteuspto-grants-2010_02