HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873557Generated: October 31, 2026
Hydrochloric Acid → HCID 131732565, compound
https://huagongshe.com/reaction/873557
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Trifluoroacetic acid water | HCID 22392675 | — |
| Reactant | HCID 131732566 | HCID 131732566 | — |
| Product | HCID 131732565 | HCID 131732565 | — |
Reaction Steps
Boc-NMe-CH2CH2—NH-Fmoc (520 mg, 1.31 mmol) was treated with TFA-water (15 ml, 95:5, v/v) for 1 hour at ambient temperature, when TLC analysis showed complete Boc-deprotection. TFA-water was removed under reduced pressure and the resulting oil dissolved in DCM (30 mL). To this solution, succinic anhydride (131 mg, 1.31 mmol) was added followed by DIPEA (to pH ˜10 by moist pH paper). The mixture was then stirred for 30 min. The reaction mixture was then acidified (pH=1) with HCl (1 M) and extracted with EtOAc (100 mL×3). The combined EtOAc layers were washed with brine (100 mL×2) and dried over Na2SO4. The EtOAc was removed under reduced pressure to give the title compound as a colorless oil. ES-MS (MeOH-direct infusion) Calculated MH+ (C23H26N2O5H+)=411.10, Observed MH+411.09.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975404B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-0dc3b92c2b0345b880a39d3efb68e700 |
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| Source note | uspto-grants-2015_03 |
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