HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865475Generated: October 31, 2026
Sodium borohydride → HCID 68682724, compound
https://huagongshe.com/reaction/1865475
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Toluene hexane | HCID 21889329 | — |
| Reactant | HCID 68681688 | HCID 68681688 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68682724 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07626056B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-d8f96ec8c451492085db4d6c9a3d9b62 |
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| Source note | uspto-grants-2009_12 |
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