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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14271Generated: October 25, 2026

Dimethyl Sulfoxide → N-(tert-Butoxycarbonyl)-D-prolinal

https://huagongshe.com/reaction/14271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantN-(tert-Butoxycarbonyl)-D-prolinolHCID 688279—
SolventDichloromethaneHCID 6344—
ProductN-(tert-Butoxycarbonyl)-D-prolinalHCID 700915380.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Oxalyl chloride (9.0 mL, 100 mmol) was added to a solution of DMSO (10.5 mL, 150 mmol) in 80 mL of CH2Cl2 at −78° C., under a nitrogen atmosphere. The solution was stirred for 20 min at −78° C., tert-butyl (2R)-2-(hydroxymethyl)pyrrolidine-1-carboxylate (9.9 g, 49 mmol) was added, and the resultant solution stirred at −78° C. for 20 min. Triethylamine (28 mL, 200 mmol) was added to the reaction solution, the dry ice-acetone bath was removed, and the resultant solution was allowed to stir for two hours, slowly warming to ambient temperature. The reaction solution was quenched with brine, the phases were separated, and the organic phase was washed with 1 M KH2PO4 and saturated NaHCO3. The organic solution was then dried over Na2SO4, filtered, and concentrated to an orange oil. This oil was then dissolved in heptane, filtered through a plug of silica gel eluting with heptane, and the filtrate was concentrated to yield tert-butyl (2R)-2-formylpyrrolidine-1-carboxylate (7.87 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-2813a31ffbc947819b5df1b62d6deea1
Source noteuspto-grants-2010_06