HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333473Generated: October 26, 2026
HCID 59189493, compound → HCID 86639081, compound
https://huagongshe.com/reaction/333473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59189493 | HCID 59189493 | — |
| Reactant | (1s)-Camphanoyl chloride | HCID 71432218 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86639081 | HCID 86639081 | 91% |
Reaction Steps
Under a nitrogen atmosphere, (1S)-camphanic acid chloride (1.68 g, 7.77 mmol) was added to a solution of (RS)-1-(4-iodo-2-nitrophenyl)-2,2-dimethyl-1-propanol (2.17 g, 6.47 mmol) and DMAP (1.18 g, 9.7 mmol) in anhydrous dichloromethane (50 mL). The mixture was stirred overnight at room temperature and then washed with saturated NaHCO3 solution (60 mL) and water (60 mL). The organic phase was dried over Na2SO4, concentrated in vacuo and purified by silica gel column chromatography to yield (RS)-1-(4-iodo-2-nitrophenyl)-2,2-dimethyl-1-propyl (1S)-camphanate (2.94 g, 88%, 1:1 mixture of diastereomers) as a white solid. 1H NMR (400 MHz, CDCl3) for diastereomers: δ 8.23 (m, 1H, Ph-H), 7.90 (m, 1H, Ph-H), 7.31 (m, 1H, Ph-H), 6.56 and 6.51 (2 s, 1H, Ph-CH), 2.38 (m, 1H), 2.07-1.9 (m, 2H), 1.69 (m, 1H), 1.13, 1.11, 1.07, 1.04, 1.02, 0.87 (6 s, 9H, CH3×3), 0.96 (s, 9H, (CH3)3C).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877905B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-8876058ab908486da08462309b875123 |
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| Source note | uspto-grants-2014_11 |
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