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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236797Generated: October 30, 2026

Ammonia → HCID 15700638, compound

https://huagongshe.com/reaction/236797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBenzoic AcidHCID 243—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15700643HCID 15700643—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
ProductHCID 15700638HCID 1570063862.9%

Reaction Steps

40.2 g (0.33 mol) of benzoic acid are added to 100 milliliters of absolute benzene and, by cooling and stirring, 3.78 g (0.1 mol) of NaBH4 are added in portions sufficiently slowly for the temperature not to exceed 20° C. After the addition of 6.3 g (20 mmol) of 3-benzylamino-2-phenyl-benzo(b)thiophene the mixture is refluxed for 60 minutes. The still hot reaction mixture has added to it by stirring half a liter of water and is neutralised by ammonia. By evaporating the organic phase dried over K2CO3 and recrystallising the residue in ethanol, 5.1 g (41% of theory) of 3-dibenzylamino-2-phenyl-benzo(b)thiophene are obtained, colourless crystals, mp 98°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04157399
Source datasetuspto-grants-1979_06
ORD IDord-1006fa3876e342159d0d645667f7e407
Source noteuspto-grants-1979_06