HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 978483Generated: October 30, 2026
Hydrochloric Acid → HCID 131714828, compound
https://huagongshe.com/reaction/978483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 13851160 | HCID 13851160 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 131714828 | HCID 131714828 | — |
Reaction Steps
To a stirred solution of 4[2-(2-[3-chlorophenyl]morpholino)propyl]phenoxy-N-methylacetamide (3.6 g) in dry tetrahydrofuran (80 ml) was added borane-methyl sulphide complex (10 ml) in dry tetrahydrofuran (20 ml), under nitrogen. The solution was boiled under reflux for 4 hours, and, after cooling to room temperature, methanol (30 ml) was added carefully. This solution was allowed to stand overnight at room temperature, hydrogen chloride gas passed through for 10 mins, boiled under reflux for one hour, cooled and evaporated to dryness. Aqueous sodium carbonate was added to the residue and extracted with dichloromethane (×2). The combined organic extracts were washed with brine (×2), dried over magnesium sulphate, filtered and evaporated to dryness. Ethereal hydrogen chloride was added to the residue and the resultant solid recrystallised from methanol-ethyl acetate to give the title compound, m.p. 145°-55° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04665072 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-dc4e57da4c5d49ccb3091b2984ede435 |
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| Source note | uspto-grants-1987_05 |
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