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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212228Generated: November 1, 2026

Dimethyl Sulfoxide → HCID 57451421, compound

https://huagongshe.com/reaction/2212228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantMonosodium phosphateHCID 23672064—
ReactantHCID 86593163HCID 86593163—
SolventDichloromethaneHCID 6344—
ProductHCID 57451421HCID 5745142192.4%

Reaction Conditions

Temperature-60 °C

Reaction Steps

A solution of oxalyl chloride (15.24 g, 120 mmol) in 200 mL of MeCl2 was stirred and cooled to −60° C. followed by the drop wise addition of dimethylsulfoxide (19.7 g, 252 mmol) in 60 mL of MeCl2. After 10 min, a solution of 2-Boc-amino-2-methyl-1-propanol (18.9 g, 100 mmol) in MeCl2 (60 mL) was added drop wise at −70° C. The reaction mixture was allowed to warm to −40° C. for 10 min followed by cooling to −70° C. before the addition of a solution of triethylamine (28.28 g, 280 mmol) in MeCl2 (60 mL). The reaction mixture was allowed to warm to room temperature over a two-hour period and 40 mL of saturated sodium dihydrogen phosphate was added. The organic layer was washed with brine and dried over MgSO4. The solvent was removed to yield 17.3 g of 2-Boc-amino-2-methylpropionaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101880B2
Source datasetuspto-grants-2006_09
ORD IDord-12530df7cb574c70b888d4ec8b71e7c1
Source noteuspto-grants-2006_09