HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022527Generated: November 2, 2026
Aluminium lithium hydride → HCID 66975707, compound
https://huagongshe.com/reaction/1022527
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 66974911 | HCID 66974911 | — |
| Reactant | HCID 66975969 | HCID 66975969 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66975707 | HCID 66975707 | 119.9% |
Reaction Steps
To a solution of lithium aluminum hydride (644 mg) in THF (40 mL) was added dropwise a solution of (6RS,7RS)-4-benzyl-6-({[tert-butyl(dimethyl)silyl]oxy}methyl)-7-(3,4-dichlorophenyl)-1,4-oxazepan-3-one (4.17 g) in THF (20 mL) under ice-cooling, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was cooled to −78° C., a solution of methyl (2R,3S)-2-[(benzylamino)methyl]-3-(3,4-dichlorophenyl)-3-hydroxypropanoate (10.8 g) in THF (80 mL) was added dropwise, and the mixture was stirred at 0° C. for 3 hr. The reaction mixture was poured into ice water, and the mixture was stirred for 30 min, and filtered through celite. The filtrate was extracted twice with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the title compound (3.44 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722662B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-c6460a84f07b4b45a81c906b681b77ae |
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| Source note | uspto-grants-2014_05 |
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