HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844874Generated: October 30, 2026
Sulfuric Acid → N-(benzyloxycarbonyl)-4-iodo-3-methyl-L-phenylalanine methyl ester
https://huagongshe.com/reaction/844874
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | n-(Benzyloxycarbonyl)-4-amino-3-methyl-l-phenylalanine methyl ester hydrochloride salt | HCID 69336581 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-(benzyloxycarbonyl)-4-iodo-3-methyl-L-phenylalanine methyl ester | HCID 69336706 | 64% |
Reaction Steps
A suspension of sulfuric acid (0.3 mL), water (36 mL) and N-(benzyloxycarbonyl)-4-amino-3-methyl-L-phenylalanine methyl ester hydrochloride salt (2.9 mmol, 1.1 g) was heated to obtain a clear solution. Then, it was cooled to −1° C. (ice-bath) and a solution of sodium nitrite (5.8 mmol, 400 mg) in water (8 mL) was added dropwise. The reaction mixture was stirred for 30 min, and a solution of potassium iodide (8.7 mmol, 1.5 g) in water (6 mL) was added to obtain a brown suspension. After stirring for 30 min, the reaction mixture was allowed to warm to room temperature and was stirred for 1 h. Then, the reaction mixture was diluted with water (100 mL) and was extracted with ethyl acetate (3×50 mL). The combined extracts were washed with saturated sodium bisulfite solution (100 mL) and brine solution (100 mL) and were dried over anhydrous magnesium sulfate. Filtration of the drying agent and concentration gave a crude product, which was purified by silica gel chromatography using a Biotage (40m) column to afford 0.84 g (64% yield) of N-(benzyloxycarbonyl)-4-iodo-3-methyl-L-phenylalanine methyl ester as an amorphous white solid. ES-HRMS m/e calcd for C19H20INO4 (M+Na) 476.0329, found 476.0336.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06380387B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-1ba49bb172ec47318957736e1ff5ba73 |
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| Source note | uspto-grants-2002_04 |
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