HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889153Generated: October 31, 2026
Benzyl chloroformate → Tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-methoxyphenyl)propanoate
https://huagongshe.com/reaction/1889153
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Tert-butyl 2-amino-3-(4-hydroxy-3-methoxyphenyl)propanoate | HCID 58545613 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-methoxyphenyl)propanoate | HCID 58545693 | 59% |
Reaction Steps
Prepared using General Procedure 2: To a stirred solution of tert-butyl 2-amino-3-(4-hydroxy-3-methoxyphenyl)propanoate INT-1 (5.29 g, 19.8 mmol) and TEA (4.29 mL, 29.7 mmol) in DCM (50 mL) at 0° C. was treated with benzyl carbonochloridate (3.00 mL, 21.1 mmol) dropwise over 5 min. After stirring for 10 min, the mixture was washed with 1M HCl (150 mL), dried over MgSO4, and concentrated. The residue was taken up in MeOH (20 mL) and treated with 2 N NaOH (5 mL). After 10 min, the mixture was acidified and the product was purified by chromatography (EA/hexanes) to afford 4.7 g (59%) of tert-butyl 2-(((benzyloxy)carbonyl)amino)-3-(4-hydroxy-3-methoxyphenyl)propanoate INT-2. LCMS-ESI (m/z) calculated for C22H27NO6: 401; found 424 [M+Na]+, tR=2.47 min (Method 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501982B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-b53e70302ed34f15b6c7730f57a6b52a |
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| Source note | uspto-grants-2013_08 |
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