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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652294Generated: October 30, 2026

Hydrochloric Acid → 2-(Phenylthiomethyl)pentane-1,5-diamine

https://huagongshe.com/reaction/652294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
Reactant2-[(Phenylsulfanyl)methyl]pentanedinitrileHCID 10059179—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-(Phenylthiomethyl)pentane-1,5-diamineHCID 20199871—

Reaction Steps

A solution of 2-(phenylthiomethyl)glutaronitrile (3.0 g.) in tetrahydrofuran (30 ml.) was stirred under an argon atmosphere while adding 10M borane-dimethyl sulphide complex (3 ml.), and the mixture was stirred at room temperature for 48 hours. The resulting gelatinous mass was treated with methanol (50 ml.) added over 1 hour and the mixture was stirred until a clear solution was obtained. The solution was acidified with a solution of hydrogen chloride in diethyl ether and then evaporated to dryness. The residue was partitioned between water and diethyl ether, and the aqueous phase was basified with 10N aqueous sodium hydroxide and then extracted three times with ether. The combined ether extracts were dried and then evaporated to dryness. The residue was purified by column chromatography on silica gel (150 g.) eluting with a mixture of ethyl acetate/methanol/concentrated ammonia, 6:1:0.5 (v/v) to give 2-(phenylthiomethyl)pentane-1,5-diamine characterised as the dihydrochloride, m.p. 166°-169°, after crystallisation from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04670592
Source datasetuspto-grants-1987_06
ORD IDord-f951866623604f40b6a08b0ee68969d5
Source noteuspto-grants-1987_06