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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643462Generated: November 2, 2026

Triethylamine → N-Boc-3-mesyloxypiperidine

https://huagongshe.com/reaction/1643462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Boc-3-hydroxypiperidineHCID 545699—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductN-Boc-3-mesyloxypiperidineHCID 568122—

Reaction Steps

1-Boc-3-hydroxypiperidine (0.5 g, 2.49 mmol) was dissolved in tetrahydrofuran (5 ml), triethylamine (0.75 g, 7.46 mmol) was added and the mixture was cooled. Methanesulfonic acid chloride (0.23 ml, 3 mmol) was added, the mixture was stirred in an ice bath for 10 min, saturated sodium bicarbonate solution (10 ml) was then added, as well as ethyl acetate (10 ml). Phase separation, the aqueous phase was extracted with ethyl acetate (2×20 ml) and the combined organic phases were washed with saturated sodium chloride solution (20 ml), dried over sodium sulfate and concentrated in vacuo. Yield: 0.54 g (77%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119805B2
Source datasetuspto-grants-2012_02
ORD IDord-1a4ff3d83ac140b98f8b7d68a67873d3
Source noteuspto-grants-2012_02