HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704611Generated: October 31, 2026
Ammonium Chloride → HCID 15735660, compound
https://huagongshe.com/reaction/704611
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Chloromethyl pivalate | HCID 87885 | — |
| Reactant | HCID 15735587 | HCID 15735587 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | DCM MeOH AcOH | HCID 21877243 | — |
| Product | HCID 15735660 | HCID 15735660 | 64.4% |
Reaction Steps
To a solution of 100 mg (0.347 millimole) of (Z)-3-cyclohexyl-2-(hydroxyisobutylphosphinoyl)methylpropenoic acid in 1.0 ml of dimethylformamide were added 130 μl (0.87 millimole) of 1,8-diazabicyclo[5,4,0]-7-undecene and 75 μl (0.52 millimole) of chloromethyl pivalate, and the mixture was stirred at room temperature for 21 hours. Fifty milliliters of a saturated aqueous solution of ammonium chloride was added to the reaction mixture, and the mixture was extracted three times with 30 ml of ethyl acetate each time. The combined organic layers were washed with 10 ml of a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by preparative thin-layer chromatography silica gel 60 F254 made by E. Merck & Co.; dichloromethane/methanol/acetic acid [30:1:1)] to give 90 mg (yield 64%) of the captioned compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988681 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-8556b961c32b43c797607a00d6d7b13e |
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| Source note | uspto-grants-1991_01 |
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