HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249178Generated: October 29, 2026
Hydrochloric Acid → benzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrate
https://huagongshe.com/reaction/249178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-[3-(3-Tert-butoxycarbonylaminobenzoyl)indol-1-yl]butyric acid | HCID 19024725 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | benzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrate | HCID 19024831 | 96.9% |
Reaction Steps
60% Sodium hydride in mineral oil (0.13 g) was added to a solution of 4-[3-(3-tert-butoxycarbonylaminobenzoyl)indol-1-yl]butyric acid (0.47 g) in N,N-dimethylformamide (7 ml). The mixture was stirred at 0° C. for 1 hour. Benzyl bromide (0.95 g) was added to the mixture and the ixture was stirred at room temperature for 20 hours. The mixture was poured into ice water and 0.5N-hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (30 g) eluting with a mixture of n-hexane and ethyl acetate (5:1) to give benzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrate (325 mg) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212320 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-44c45fc83b574a23a0d4d17f24fd0b31 |
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| Source note | uspto-grants-1993_05 |
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