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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587645Generated: October 26, 2026

Ammonium Chloride → 1'-(benzyl)-spiro[isobenzofuran-1(3H),4'-piperidin]-3-thione

https://huagongshe.com/reaction/587645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLawesson's reagentHCID 87949—
Reactant1'-Benzyl-3H-spiro[isobenzofuran-1,4'-piperidin]-3-oneHCID 10266406—
SolventTolueneHCID 1140—
Product1'-(benzyl)-spiro[isobenzofuran-1(3H),4'-piperidin]-3-thioneHCID 86667988—

Reaction Conditions

Temperature140 °C

Reaction Steps

To a mixture of 1′-(phenylmethyl)-spiro[isobenzofuran-1(3H),4′-piperidin]-3-one (25 g, 85.2 mmol) [C.A.S. 37663-42-6] in toluene (600 ml), was added 2,4-bis(4-methoxyphenyl)-1,3-dithia-2,4-diphosphetane 2,4-disulfide (Lawesson's reagent) (34.47 g, 85.2 mmol was added. The reaction mixture was heated at 140° C. for 2 h. After cooling, the mixture was poured into NH4Cl (aqueous sat. solution) and extracted with DCM. The organic phase was separated, dried (MgSO4) and concentrated in vacuo. The residue was purified by column chromatography (silica gel; DCM/MeOH 3% as eluent). The desired fractions were collected and concentrated in vacuo to a residue that was purified by HPLC to yield intermediate D72 (8 g, 30.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226930B2
Source datasetuspto-grants-2016_01
ORD IDord-10381f41c8724e6e96622a5b93b27e10
Source noteuspto-grants-2016_01