Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757303Generated: November 3, 2026

Methanesulfonyl chloride → HCID 13857264, compound

https://huagongshe.com/reaction/1757303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-Boc-D-phenylalaninolHCID 7019371—
SolventDichloromethaneHCID 6344—
ProductHCID 13857264HCID 13857264—

Reaction Steps

To a solution of N-tert-butoxycarbonyl-D-Phenylalaninol (754 mg) and TEA (0.5 ml) in dichloromethane was added methanesulfonyl chloride (0.28 ml) at 0°~5 ° C. The reaction mixture was stirred at 0°~5 ° C. for 30 min, quenched with water, and extracted with dichloromethane. The organic layer was washed with 10% citric acid and sat. NaHCO, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was crystallized from ethyl acetate/hexane=1/2 to afford the product (931 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05444152
Source datasetuspto-grants-1995_08
ORD IDord-2d1093498fbf46b4a0c1eae13bfacfbd
Source noteuspto-grants-1995_08