Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12405Generated: October 27, 2026

Triethylamine → (S)-Methanesulphonic acid 2-Boc-aminopropyl ester

https://huagongshe.com/reaction/12405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,1-Dimethylethyl N-((1S)-2-hydroxy-1-methylethyl)carbamateHCID 7023103—
SolventDichloromethaneHCID 6344—
Product(S)-Methanesulphonic acid 2-Boc-aminopropyl esterHCID 10753379—

Reaction Conditions

Temperature0 °C

Reaction Steps

To the compound (5.9 g) obtained in Step 1 were added methanesulfonyl chloride (3.1 ml), triethylamine (9.0 ml) and dichloromethane (150 ml), and the mixture was stirred at 0° C. for 2 hrs. The mixture was diluted with dichloromethane and, after washing with water, the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated to give the title compound as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728005B2
Source datasetuspto-grants-2010_06
ORD IDord-6f5c4f28190c47c0b1aa9429d8e223c6
Source noteuspto-grants-2010_06