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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280178Generated: October 30, 2026

Piperidine → HCID 20137131, compound

https://huagongshe.com/reaction/280178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20137123HCID 20137123—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 20137131HCID 20137131—

Reaction Conditions

Temperature0 °C

Reaction Steps

Triethylamine (10 ml) is added to a stirred solution of the 1-hydroxy indane of Step 2. above (8.4 g) in methylene chloride (190 ml) at RT under nitrogen; the mixture is cooled to 0° C. and methanesulfonyl chloride (4 ml) is added. The mixture is stirred for three hours at RT, cooled to 0° C., piperidine (128 ml) added and stirred at RT overnight. Sat'd aq. sodium bicarbonate is added to the mixture and the organic phase separated, washed with aq. sodium bicarbonate, sat'd NaCl, dried, filtered and the filtrate evaporated in vacuo affording the desired product as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04588719
Source datasetuspto-grants-1986_05
ORD IDord-00aad20b01024b28b35d8cd9f127559c
Source noteuspto-grants-1986_05