HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731554Generated: October 30, 2026
Methanol → (R)-4-Morpholino-1-(phenylthio)-2-butylamine
https://huagongshe.com/reaction/731554
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Borane | HCID 6331 | — |
| Reactant | (R)-3-amino-1-morpholino-4-(phenylthio)butan-1-one | HCID 59186675 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-4-Morpholino-1-(phenylthio)-2-butylamine | HCID 25058453 | 73% |
Reaction Steps
A solution of EXAMPLE 21E (6.00 g, 21.4 mmol) in THF (80 mL) was heated to 55° C. and treated dropwise with a solution of 1M borane in THF (85 mL, 85.0 mmol) over a 1 hour period. The resulting reaction mixture was stirred at 55° C. for 18 hours, cooled to 0° C., treated dropwise with methanol (10 mL), treated with 150 mL additional methanol, and concentrated. The crude residue was dissolved in methanol (70 mL), treated with methanolic HCl (100 mL), and heated to reflux for 24 hours. The mixture was allowed to cool to room temperature, concentrated, diluted with 2M NaOH (200 mL), and extracted with ethyl acetate (3×250 mL). The combined extracts were washed with 1M NaOH and brine, dried (Na2SO4), filtered, concentrated, and purified by silica gel chromatography eluting with 5% triethylamine/10% methanol/0% acetonitrile/ethyl acetate to provide the desired product (3.45 g, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585858B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-a6804548d7e746a8876feb7a45dc0c59 |
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| Source note | uspto-grants-2009_09 |
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