HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565248Generated: October 29, 2026
Acetic-formic anhydride → HCID 57151785, compound
https://huagongshe.com/reaction/565248
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic-formic anhydride | HCID 75269 | — |
| Reactant | HCID 57246922 | HCID 57246922 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57151785 | HCID 57151785 | 91% |
Reaction Steps
To a solution of (2R,3S)-2-(3-(thiophene-2-yl)-1-propyl)-3-(2-tetrahydropyranyloxyamino)butanoic acid (91 mg, 0.278 mmol) in pyridine (1 mL) at 0° C. is added formic acetic anhydride (0.3 mL). The resulting solution is allowed to warm to 25° C., stirred for 3 h, and then concentrated to dryness under reduced pressure. The resulting gum is dissolved in ethyl acetate (30 mL) and washed sequentially with 1 M hydrochloric acid (20 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-(thiophene-2-yl)-1-propyl)-3-(formyl-2-tetrahydropyranyloxyamino)butanoic acid as an oil (90 mg, 91% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06172064B2 |
|---|
| Source dataset | uspto-grants-2001_01 |
|---|
| ORD ID | ord-ae68e65aa78f4e9e99b8ab02907b5590 |
|---|
| Source note | uspto-grants-2001_01 |
|---|