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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865475Generated: October 31, 2026

Sodium borohydride → HCID 68682724, compound

https://huagongshe.com/reaction/1865475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantToluene hexaneHCID 21889329—
ReactantHCID 68681688HCID 68681688—
ReactantHCID 178418573HCID 178418573—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductHCID 68682724HCID 68682724—

Reaction Steps

1-(cyclopropylmethyl)4-[(cyclopropylmethyl)thio]cyclohexanecarbonitrile (2 g; 8.0321 mmol) was dissolved in toluene (30 mL) and methylmagnesium bromide (8.6 ml; 12mL of a 1.4M solution in 3:1 toluene/hexane) was added and the reaction mixture was heated to reflux for 16 hours. The reaction was cooled to 0C. and methanol (12 mL) was added and the mixture was stirred for 15 minutes before adding sodium borohydride (0.315 g; 8.514026 mmol) and stirring for 0.5 hours at room temperature. The reaction was carefully quenched with 1 M hydrochloric acid (24 mL) and then extracted into ethyl acetate and purified using a 40M Biotage cartridge using 5% (2M ammonia in methanol)/DCM to yield (1-{1-(cyclopropylmethyl)-4-[(cyclopropylmethyl)thio]cyclohexyl}ethyl)amine. (1.6 g, 75%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07626056B2
Source datasetuspto-grants-2009_12
ORD IDord-d8f96ec8c451492085db4d6c9a3d9b62
Source noteuspto-grants-2009_12