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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499221Generated: October 25, 2026

Triethylamine → N-BOC-3(R)-methylsulfonyloxymethyl-piperidine

https://huagongshe.com/reaction/499221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-butyl (3R)-3-(hydroxymethyl)piperidine-1-carboxylateHCID 1514447—
SolventDichloromethaneHCID 6344—
ProductN-BOC-3(R)-methylsulfonyloxymethyl-piperidineHCID 10108453—

Reaction Conditions

Temperature0 °C

Reaction Steps

2.16 ml of methanesulphonyl chloride followed by 3.86 ml of triethylamine are added to a solution of 5 g of (R)-3-hydroxymethylpiperidine-1-carboxylic acid tert-butyl ester in 80 ml of DCM cooled to 0° C. The medium is stirred at 0° C. for 1 h 30 min and 0.7 ml of triethylamine and 0.54 ml of methanesulphonyl chloride are again added. After 30 min at 0° C., the medium is hydrolysed, and the organic phase is washed twice in water and then with a saturated NaCl solution, and then dried over MgSO4. The medium is evaporated, to give 6.8 g of a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767681B2
Source datasetuspto-grants-2010_08
ORD IDord-f0d21d91905148a0af67c3a60fc88b44
Source noteuspto-grants-2010_08