HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256527Generated: October 31, 2026
Thionyl Chloride → 4-(Chloromethyl)-N-methyl-2-nitroaniline
https://huagongshe.com/reaction/256527
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | [4-(Methylamino)-3-nitrophenyl]methanol | HCID 12323420 | — |
| Product | 4-(Chloromethyl)-N-methyl-2-nitroaniline | HCID 10976511 | 55% |
Reaction Steps
1.0 g (5.5 mmol) of 9 was dissolved in 25 ml thionylchloride at -78° C. cooled with dry ice/acetone bath. After it dissolved completely, the dry ice/acetone bath was removed and the reaction mixture allowed to warm up to room temperature and kept at room temperature for additional 1 hour. Thionylchloride was evaporated under vacuum at room temperature and the residue was washed with 5 ml cold diethylether and recrystallized from diethylether to yield 0.6 g (55%) of 10. Yellow, mp: 126°-128° C. 1H NMR: (DMSO-d6): δ 82.9 (s, 1H, NH), 8.15 (d, 1H, J=2.2 Hz, H-2), 7.60p, 1H, (dd, 1H, J=8.9, 2.2 Hz, H-6), 7.01 (d, 1H, J=9.0 Hz, H-5), 4.76 (s, 3H, CH2), 2.95 (s, 3H, CH3). Anal. Calcd for C8H9N2O2Cl: C, 47.89; H, 4.52; Cl, 17.67; N, 14.00; O, 15.95. found: C, 47.78; H, 4.49; Cl, 17.78; N, 13.82; O, 16.13.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05258370 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-819b806217ff444191a6f31ac531eb15 |
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| Source note | uspto-grants-1993_11 |
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