HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975933Generated: October 30, 2026
Ammonia → (+/-)-4-Methyl-6-methoxy-9-iodo3,4,4a,5,10,10a-hexahydro-2H-naphto-[2,3-b][1,4]oxazine
https://huagongshe.com/reaction/975933
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 4-methyl-6-methoxy-3,4,4a,5,10,10a-hexahydro-2H-naphtho[2,3-b][1,4]oxazine | HCID 15131079 | — |
| Reactant | Ethylacetate methanol | HCID 21584119 | — |
| Catalyst | Diacetyloxymercury | HCID 16683746 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (+/-)-4-Methyl-6-methoxy-9-iodo3,4,4a,5,10,10a-hexahydro-2H-naphto-[2,3-b][1,4]oxazine | HCID 15131081 | 44% |
Reaction Steps
A solution of 4-methyl-6-methoxy-3,4,4a,5,10,10a-hexahydro-2H-naphtho[2,3-b][1,4]oxazine (0.37 g, 1.6 mmol) was dissolved in 7 ml of AcOH and heated to 50° C. To the solution of the amine was added a solution of Hg(OAc)2 (0.62 g, 19 mmol) and I2 (1.0 g, 3.8 mmol) in 30 ml of AcOH. The resulting solution was stirred for 1 h at 50° C. and 1.5 h at 25° C. The reaction mixture was filtered to remove mercury salts and concentrated in vacuo, yielding an oily residue which was subjected to column chromatography (5% NH3 sat'd MeOH-EtOAc) to yield 0.25 g (44%) of the desired product. 1H NMR (300 MHz, CDCl3): δ 2.04 (m, 1H), 2.32 (dd, 1H, J=11.0, 18.0 Hz), 2.41 (s, 3H), 2.49 (m, 1H), 2.62 (dd, 1H, J=11.0, 17.0 Hz), 2.76 (m, 1H), 3.12 (dd, 1H, J=6.0, 17.0 Hz), 3.33 (dd, 1H, J=5.6, 17.0 Hz), 3.56 (m, 1H), 3,81 (s, 3H), 3.88 (m, 2H), 6.47 (d, 1H, J=7.8 Hz), 7.66 (d, 1H, J=7.8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05610174 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-0c38da2546864177a396523135e649b7 |
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| Source note | uspto-grants-1997_03 |
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