HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565234Generated: October 30, 2026
Acetic-formic anhydride → HCID 11245009, compound
https://huagongshe.com/reaction/565234
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic-formic anhydride | HCID 75269 | — |
| Reactant | HCID 57245995 | HCID 57245995 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 11245009 | HCID 11245009 | 81% |
Reaction Steps
To a solution of (2R,3S)-2-(3-phenyl-1-propyl)-3-(2-tetrahydropyranyloxyamino)butanoic acid (21.4 g, 66.7 mmol) in pyridine (100 mL) at 0° C. is added formic acetic anhydride (30 mL). The resulting solution is allowed to warm to 25° C., stirred for 6 h, and then concentrated to dryness under reduced pressure. The resulting gum is dissolved in ethyl acetate (300 mL) and washed sequentially with 1 M hydrochloric acid (200 mL) and saturated aqueous sodium chloride solution. The organic layer is dried over anhydrous magnesium sulfate and concentrated under reduced pressure to provide (2R,3S)-2-(3-Phenyl-1-propyl)-3-(formyl-2-tetrahydropyranyloxyamino)butanoic acid as an oil (18.9 g, 81% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172064B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-bb92def3ddca4b93a5bcf89f92d4376e |
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| Source note | uspto-grants-2001_01 |
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