HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558938Generated: October 30, 2026
Ammonia → 4-{[(tert-Butoxycarbonyl)amino]methyl}-3-chlorobenzoic acid
https://huagongshe.com/reaction/558938
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Methyl 4-(bromomethyl)-3-chlorobenzoate | HCID 22027761 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-{[(tert-Butoxycarbonyl)amino]methyl}-3-chlorobenzoic acid | HCID 22027774 | — |
Reaction Steps
To a saturated solution of ammonia in ethanol (170 ml) was added methyl 4-bromomethyl-3-chlorobenzoate from Example A1 (5.5 g, 20.9 mmol). The mixture was stirred at room temperature for 1 hr and then concentrated in vacuo. The residue was triturated with diethyl ether and the resultant white crystals were filtered off and washed with more diethyl ether. To a solution of this solid in water (100 ml) were added solutions of (BOC)2O (5.0 g, 23.0 mmol) in dioxan (100 ml) and sodium hydroxide (1.86 g, 46.0 mmol) in water (100 ml). The mixture was stirred at room temperature for 18 h and then concentrated in vacuo. The aqueous residue was acidified with citric acid and extracted with chloroform/IPA. The organic layer was washed with water, dried over MgSO4, and concentrated in vacuo to give a white solid; yield 2.8 g (67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063038B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-bb942c15be0f48248e1548199354864b |
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| Source note | uspto-grants-2011_11 |
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