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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium ThiosulfateHCID 24477—
Reactant1-(Benzyl(2-methylallyl)amino)-2-methylpropan-2-olHCID 57421496—
Solventtert-Butyl methyl etherHCID 15413—
SolventSodium BicarbonateHCID 516892—
Product4-Benzyl-2-(iodomethyl)-2,6,6-trimethylmorpholineHCID 5742149793%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902356B2
Source datasetuspto-grants-2011_03
ORD IDord-580b45cd0ea644bf879574c4a0ad14e8
Source noteuspto-grants-2011_03