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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363573Generated: October 30, 2026

3-(Trifluoromethyl)benzenesulfonyl chloride → HCID 66590601, compound

https://huagongshe.com/reaction/2363573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2733250—
Reactant4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
Reactant(3aR,4S,6aS)-2-benzyloctahydrocyclopenta[c]pyrrol-4-amineHCID 66591011—
ProductHCID 66590601HCID 66590601—

Reaction Steps

(3aS,4R,6aR)-2-(4-(Trifluoromethyl)phenylsulfonyl)octahydrocyclopenta[c]pyrrol-4-amine was prepared by following the procedures described in Example 252 Steps A-D substituting (3aS,4R,6aR)-2-benzyloctahydrocyclopenta[c]pyrrol-4-amine from Step E of Example 16 for (3aR,4S,6aS)-2-benzyloctahydrocyclopenta[c]pyrrol-4-amine in Step A of Example 252 and 4-(trifluoromethyl)benzene-1-sulfonyl chloride for 3-(trifluoromethyl)benzene-1-sulfonyl chloride in the procedure described in Step C of Example 252: 1H NMR (500 MHz, pyridine-d5) δ ppm 8.15 (d, J=8.2, 2H), 7.92 (d, J=8.3, 2H), 3.40 (dd, J=9.8, 2.9, 1H), 3.13 (dd, J=9.7, 3.2, 1H), 3.06-2.93 (m, 3H), 2.54 (s, 1H), 2.21-2.12 (m, 1H), 1.93-1.85 (m, 1H), 1.78-1.69 (m, 1H), 1.67-1.33 (m, 2H), 1.33-1.15 (m, 2H); MS (ESI+) m/z 335 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691865B2
Source datasetuspto-grants-2014_04
ORD IDord-3f1c5cb1b2904efc9f29163b075b5ed3
Source noteuspto-grants-2014_04