HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222449Generated: October 29, 2026
Hydrochloric Acid → ethyl (4R)-4-(tert-butoxycarbonylamino)-4-formylbutanoate
https://huagongshe.com/reaction/222449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl (4R)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentanoate | HCID 57351319 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ethyl (4R)-4-(tert-butoxycarbonylamino)-4-formylbutanoate | HCID 57894011 | 98.8% |
Reaction Steps
Under atmosphere of argon, to a solution of (4R)-5-hydroxy-4-t-butoxycarbonylaminopentanoic acid ethyl ester (15.0 g), triethylamine (32.0 mL) and dimethylsulfoxide (39 mL) in ethyl acetate (120 mL), a solution of sulfur trioxide pyridine complex (18.3 g) in mixed solvent ethyl acetate (30 mL) and dimethylsulfoxide (75 mL) was added at 0° C., and the mixture was stirred for 1 hour. The reaction mixture was added by water (5 mL) at 0° C. and was added by 1N hydrochloric acid (240 mL). Separated aqueous layer was extracted by ethyl acetate. The combined organic layer was washed with water and brine successively, dried over an anhydrous sodium sulfate, concentrated under reduced pressure to give the title compound (14.7 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207223B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-052e1632a2c44812bd295e9f2c245524 |
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| Source note | uspto-grants-2012_06 |
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