HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435403Generated: October 28, 2026
Tetrahydrofuran → HCID 13091049, compound
https://huagongshe.com/reaction/435403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | L-Serine, N-[(1,1-dimethylethoxy)carbonyl]-O-(phenylmethyl)- | HCID 90234 | — |
| Reactant | O-BENZYL-L-SERINE METHYL ESTER HYDROCHLORIDE | HCID 44630138 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13091049 | HCID 13091049 | 875.5% |
Reaction Steps
THF (700 ml) and BOC-Ser(Bzl)-OH (23.6 g, 0.8 M) and HOBT (108 g, 0.8 M) were added to H-Ser(Bzl)-Ome.HCl (196.57 g, 0.8 M); and DMF (200 ml) was added to prepare a solution. WSCI (146 ml, 0.8 M) was added dropwise thereto at 0° C. and the mixture was stirred at 0° C. for one hour and at room temperature overnight. The reaction mixture was concentrated in vacuo, and ethyl acetate (1 l.) was added to the residue, which was then washed with 5% sodium bicarbonate solution, 1 N HCl and water, each three times, in that order. Hexane was added to the oily product, which was then crystallized by adding crystalline seed. The material was then recrystallized from ether-hexane to obtain the substance [28] (340.4 g, yield: 87.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04400316 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-3fca5602cd2b43a4b2574f7af368fe6d |
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| Source note | uspto-grants-1983_08 |
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