HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737418Generated: November 2, 2026
4-(Trifluoromethoxy)benzylamine → HCID 10385941, compound
https://huagongshe.com/reaction/1737418
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-(Trifluoromethoxy)benzylamine | HCID 571846 | — |
| Reactant | (R)-2-(Toluene-4-sulfonyloxymethyl)-2,3,8,9-tetrahydro-7H-1,4-dioxino[2,3-e]indol-8-one | HCID 15381104 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 10385941 | HCID 10385941 | 46% |
Reaction Steps
(R)-2-(Toluene-4-sulfonyloxymethyl)-2,3,8,9-tetrahydro-7H-1,4-dioxino[2,3-e]indol-8-one (1.0 g, 2.7 mmole) and 4-trifluoromethoxybenzylamine (2.0 g, 11 mmole) were combined in 30 ml of dry DMSO and heated to 90° C. for 4 hours under an argon atmosphere. After cooling to room temperature, the mixture was diluted with 400 ml of 1:1 ethyl acetate/hexane and washed with 400 ml of saturated sodium bicarbonate solution, with two 250 ml portions of water and with saturated brine. The mixture was dried over sodium sulfate, filtered and concentrated in vacuum to yield an oil, which was column chromatographed on silica gel using 1% methanol/CHCl3 as eluant. The free base of the title compound (0.49 g) thus obtained was crystallized from ethanol with the addition of one equivalent of fumaric acid to give 0.29 g of the (S) enantiomer of the title compound as a white solid fumarate, m.p. 201-202° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962465 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-5140761727c14b43b89a3d2c9b7427ef |
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| Source note | uspto-grants-1999_10 |
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