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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278484Generated: October 30, 2026

Triethylamine → (2S,3S)-2-benzyloxy-5-(1-naphthyl)-3-pentyl methanesulfonate

https://huagongshe.com/reaction/278484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2S,3S)-2-benzyloxy-5-(1-naphthyl)pentan-3-olHCID 57094200—
SolventDichloromethaneHCID 6344—
Product(2S,3S)-2-benzyloxy-5-(1-naphthyl)-3-pentyl methanesulfonateHCID 56983838107.4%

Reaction Conditions

Temperature4 °C

Reaction Steps

To an ice-cooled solution of (2S,3S)-2-benzyloxy-5-(1-naphthyl)pentan-3-ol (obtained in Preparation 26) (7.43 g) in dichloromethane (100 ml) was added methanesulfonyl chloride (2.15 ml) followed by triethylamine (3.88 ml). The mixture was stirred at 4° C. for 40 min. After being diluted with dichloromethane, the mixture was washed with water and brine, dried and concentrated in vacuo to give (2S,3S)-2-benzyloxy-5-(1-naphthyl)-3-pentyl methanesulfonate (9.92 g, 107.4%) as an oil. The product was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06359145B1
Source datasetuspto-grants-2002_03
ORD IDord-a20ce673e54e486cb67530a62c074fd5
Source noteuspto-grants-2002_03