HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296202Generated: October 26, 2026
Sodium Carbonate → (3-Bromobenzyl)-carbamic acid 9H-fluoren-9-ylmethyl ester
https://huagongshe.com/reaction/1296202
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Bromobenzylamine hydrochloride | HCID 2724980 | — |
| Reactant | Fmoc-N-hydroxysuccinimide | HCID 21653429 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (3-Bromobenzyl)-carbamic acid 9H-fluoren-9-ylmethyl ester | HCID 67519536 | 82.1% |
Reaction Steps
To 3-bromobenzylamine hydrochloride (16.0 g, 71.9 mmol) was added aqueous 9% Na2CO3 (211 mL) followed by 9-fluorenylmethyloxycarbonyl-N-hydroxysuccinimide (25.5 g, 75.5 mmol) in dioxane (211 mL). This was stirred 30 minutes, then diluted with CH2Cl2 (200 mL). The layers were separated and the aqueous layer was extracted with CH2Cl2. The combined organic layers were washed with 1 M HCl, brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting solid was purified by recrystallization (ethyl acetate/hexanes) to obtain a fluffy, white solid (24 g, 59 mmol, 82%). 1H NMR (400 MHz, d6-DMSO): δ 7.90 (t, 1H, J=6.2 Hz), 7.88 (d, 2H, J=7.5 Hz), 7.68 (d, 2H, J=7.5 Hz), 7.43 (m, 4H), 7.32 (dd, 2H, J=7.5 Hz, 7.5 Hz), 7.26 (d, 1H, J=7.7 Hz), 7.20 (d, 1H, J=7.3 Hz), 4.35 (d, 2H, J=6.6 Hz), 4.22 (t, 1H, J=6.6 Hz), 4.17 (d, 2H, J=6.2 Hz). ESI/MS: 408 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244853B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-7e42d4a3b15d445ca0b8f8ddf5d9277c |
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| Source note | uspto-grants-2007_07 |
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