HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383119Generated: November 1, 2026
Tetrabutylammonium Fluoride → HCID 20698898, compound
https://huagongshe.com/reaction/383119
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | HCID 20698900 | HCID 20698900 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20698898 | HCID 20698898 | 57% |
Reaction Steps
To a solution of 1.82 g (2.65 mmol) of {4-[N-Boc-4-(t-butyldimethylsilyloxy)-prolinyl]amino-2-phenylbenzoyl}methionine methyl ester, prepared as in Example 169B, in 20 ml of THF was added 3 ml (3 mmol) of 1 M tetra-n-butylammonium fluoride in THF. The reaction mixture was stirred overnight, diluted with ethyl acetate, and washed 3 times with water. The combined aqueous washings were extracted 3 times with ethyl acetate. The combined organic fractions were dried over magnesium sulfate and concentrated in vacuo. The crude product was purified by flash chromatography on silica gel (ethyl acetate) to obtain 864 mg (57%) of [4-(N-Boc-4-hydroxyprolinyl)amino-2-phenylbenzoyl]methionine methyl ester as a white solid: mp 121-123° C. ; [α]25D−53.3 (c=0.43, CHCl3);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310095B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-0c4e92e2a6b540be974f50c88ce71f3f |
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| Source note | uspto-grants-2001_10 |
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