HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007709Generated: October 29, 2026
Hydrochloric Acid → HCID 178511762, compound
https://huagongshe.com/reaction/1007709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 491265 | HCID 491265 | — |
| Product | HCID 178511762 | HCID 178511762 | — |
Reaction Steps
The tetrazole compound from above (0.752 g, 2.16 mmol) was dissolved in THF (20 mL) and DIEA (0.75 mL, 4.3 mmol) and triphenylchloromethane (trityl chloride, 0.604 g, 2.16 mmol) were added. The reaction was stirred for 1 h at room temperature and then quenched with 1 N NaOH (13 mL, 13 mmol). After stirring overnight at room temperature, the reaction mixture was cooled in ice and acidified to pH 3-4 with 1 N HCl. The product was extracted into EtOAc (50 mL), washed with brine and the solution dried (Na2SO4). Evaporation of the solvent gave a yellow residue that was purified by passing through a pad of silica gel using EtOAc as eluent. The product was then dissolved in TBME (5 mL) and hexane (10 mL) was added. The precipitated material was collected by filtration and dried to give the desired 4-tetrazolyl-L-phenylalanine free acid as a white solid (0.784 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06794404B2 |
|---|
| Source dataset | uspto-grants-2004_09 |
|---|
| ORD ID | ord-9501f648f39d4e36bfca14ca73370a8f |
|---|
| Source note | uspto-grants-2004_09 |
|---|