HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 601555Generated: October 30, 2026
Iodine → 4-Benzyl-2-(iodomethyl)-2,6,6-trimethylmorpholine
https://huagongshe.com/reaction/601555
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 1-(Benzyl(2-methylallyl)amino)-2-methylpropan-2-ol | HCID 57421496 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 4-Benzyl-2-(iodomethyl)-2,6,6-trimethylmorpholine | HCID 57421497 | 93% |
Reaction Steps
Add solid I2 (21.1 g, 83.1 mmol) to a biphasic mixture of 1-[benzyl-(2-methyl-allyl)-amino]-2-methyl-propan-2-ol (17.6 g, 75.4 mmol) in tert-butyl methyl ether (250 mL) and 1 M NaHCO3 (100 mL). Stir for 18 h and then add 1 M Na2S2O3 (100 mL). Dilute the mixture with additional tert-butyl methyl ether (200 mL) and separate the organic solution. Wash the organic solution with a mixture of 1 M Na2S2O3 (100 mL) and 1M NaHCO3 (100 mL). Dry, filter, and concentrate the organic solution. Dry the residue at 60° C. under vacuum to give the title compound (25.2 g, 93%) as a golden oil. 1H NMR (400 MHz, DMSO-d6): δ 7.2-7.4 (5H, m), 3.49 (1H, d), 3.47 (2H, s), 3.41 (1H, s), 2.49 (1H, d), 2.23 (1H, s), 2.20 (1H, s), 2.10 (1H, d), 1.24 (3H, s), 1.22 (3H, s), 1.15 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902356B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-580b45cd0ea644bf879574c4a0ad14e8 |
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| Source note | uspto-grants-2011_03 |
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