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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862732Generated: October 26, 2026

Thionyl Chloride → HCID 19698661, compound

https://huagongshe.com/reaction/862732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 4-piperidinecarboxylateHCID 70770—
Reactant9,10-Dihydro-9,10-methano-9-anthracenecarboxylic acidHCID 12507119—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
ProductHCID 19698661HCID 1969866192.2%

Reaction Steps

A solution of 9,10-dihydro-9,10-methano-9-anthracenecarboxylic acid (21.8 g, 92.4 mmol) in toluene (160 mL) was treated with thionyl chloride (11.7 g, 99 mmol) and N,N-dimethylformamide (0.1 g). The resulting solution was heated to reflux temperature for 2 h, then was cooled to room temperature. The mixture was then treated dropwise with a solution of ethyl isonipecotate (31.1 g, 198 mmol) in toluene (20 mL), using an ice/water bath to keep the reaction temperature <35° C. Upon complete addition, the mixture was stirred for 1 h at room temperature, then was washed sequentially with 10% hydrochloric acid (40 mL), water (40 mL), 1N aqueous sodium hydroxide (40 mL), water (40 mL) and brine (40 mL). The aqueous washes were extracted with toluene (100 mL). The organic extracts were combined, dried (MgSO4), filtered and concentrated to afford the title compound (33.0 g, 85.2 mmol, 92%) as an off-white solid. 1H NMR (d6-DMSO): δ7.33-7.14 (m, 4H), 6.99 (m, 4H), 4.54 (br, 1H), 4.38 (s, 1H, H--C(10)), 4.09 (q, J=6.5 Hz, 2H, CH2CH3), 3.8 (br, 1H), 3.0-2.5 (br, 6H), 2.05-1.45 (br, 5H), 1.19 (t, J=6.5 Hz, 3H, CH2CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719166
Source datasetuspto-grants-1998_02
ORD IDord-c12cc8f8bbf54eb9a2f35587b1d0280c
Source noteuspto-grants-1998_02