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Chemical Structure| 873197-15-0 Chemical Structure| 873197-15-0

Structure of 873197-15-0

Chemical Structure| 873197-15-0

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Product Details of [ 873197-15-0 ]

CAS No. :873197-15-0
Formula : C16H25NO3
M.W : 279.37
SMILES Code : O=C(OC(C)(C)C)CN(CC1=CC=CC=C1)[C@@H](C)CO

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Application In Synthesis of [ 873197-15-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 873197-15-0 ]

[ 873197-15-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5292-43-3 ]
  • [ 6940-80-3 ]
  • [ 873197-15-0 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In N,N-dimethyl-formamide; at 0 - 20℃; for 19.8333h; (2) Optically-Active Compound of [benzyl-(2-hydroxy-1-methylethyl)-amino]acetic acid tert-butyl esterTo a mixture of an optically-active compound of 2-benzylaminopropan-1-ol (111.2 g), potassium carbonate (111.6 g) and N,N-dimethylformamide (556 ml) cooled to 0° C. was added dropwise bromoacetic acid tert-butyl ester (109 ml) over 20 minutes, and the mixture was stirred at room temperature for 19.5 hours. The mixture was acidified by the addition of 2M aqueous hydrochloric acid solution and 6M aqueous hydrochloric acid solution to pH 2, and washed with toluene (1000 ml). The separated organic layer was extracted with 0.1M aqueous hydrochloric acid solution (300 ml). The combined aqueous layer was adjusted to pH 10 by 4M aqueous sodium hydroxide solution, and extracted with ethyl acetate (700 ml). The organic layer was sequentially washed with water (900 ml) and saturated aqueous sodium chloride solution (500 ml). The separated aqueous layer was extracted with ethyl acetate (400 ml) again. The combined organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give the titled compound (160.0 g).1H-NMR (DMSO-D6) delta: 7.37-7.26 (4H, m), 7.24-7.19 (1H, m), 4.26 (1H, dd, J=6.9, 3.9 Hz), 3.76 (1H, d, J=14.1 Hz), 3.68 (1H, d, J=13.9 Hz), 3.45-3.39 (1H, m), 3.29-3.20 (1H, m), 3.24 (1H, d, J=17.2 Hz), 3.13 (1H, d, J=17.0 Hz), 2.84-2.74 (1H, m), 1.37 (9H, s), 0.96 (3H, d, J=6.8 Hz).
With potassium carbonate; In water; toluene; at 65℃; for 21h;Inert atmosphere; S-BAPO [1] (35.0 g, 212 mmol) was added to water (175 mL) at room temperature under nitrogen atmosphere. To the resulting suspension were added toluene (53 mL) and potassium carbonate (32.2 g, 233 mmol) at room temperature. To the resulting solution was added dropwise TBBA (434.4 g, 223 mmol) at room temperature, and then the used dropping funnel was washed with toluene (17 mL) and the washings were added to the reaction mixture. The reaction mixture was stirred at 65°C for 21 hours, and then cooled to room temperature. After toluene (105 mL) was added to the reaction mixture and then the mixture was stirred, the organic layer was separated out. The organic layer was washed with water (175 mL), aqueous layer was removed, and then the solvent was removed out of the organic layer in vacuo. Toluene (105 mL) was added to the residue and the toluene solution was concentrated. The operation was repeated two more times to give a toluene solution of S-BBMO [2] (74.0 g, 212 mmol in theory). The given toluene solution of S-BBMO was used in the next step, assuming that the yield was 100 percent. A crude product of S-BBMO which was prepared by the same process was evaporated to dryness and then measured about NMR and MS. 1H-NMR (DMSO-d 6) delta: 7.36-7.13 (5H, m), 4.26 (1H, dd, J = 6.8, 3.9 Hz), 3.72 (2H, dd, J = 14.2, 6.8 Hz), 3.47-3.38 (1H, m), 3.30-3.08 (3H, m), 2.79 (1H, sext, J = 6.8 Hz), 1.35 (9H, s), 0.96 (3H, d, J = 6.8 Hz). MS: m/z = 280 [M+H] +
With potassium carbonate; In water; toluene; at 65℃; for 21h;Inert atmosphere; 5-HAPO [1] (35.0 g, 212 mmol) was added to water (175 mE) at room temperature under nitrogen atmosphere. To the resulting suspension were added toluene (53 mE) and potassium carbonate (32.2 g, 233 mmol) at room temperature. To the resulting solution was added dropwise THEA (434.4 g, 223 mmol) at room temperature, and then a dropping thnnel used was washed with toluene (17 mE) and the washings were added to the reaction mixture. The reaction mixture was stirred at 65° C. for 21 hours, and then cooled to room temperature. Afier toluene (105 mE) was added to the reaction mixture and then the mixture was stirred, the organic layer was separated out. The organic layer was washed with water (175 mE), aqueous layer was removed, and then the solvent was removed out of the organic layer in vacuo. Toluene (105 mE) was added to the residue and the toluene solution was concentrated. The operation was repeated two more times to give a toluene solution of 5-HEMO [21(74.0 g, 212 mmol in theory). The given toluene solution of 5-HEMO was used in the next step, assuming that the yield was 100percent. A crude product of 5-HEMO which was prepared by the same process was evaporated to dryness and then measured about NMR and MS. ?H-NMR (DMSO-d5) oe: 7.36-7.13 (5H, m), 4.26 (1H, dd, J=6.8, 3.9 Hz), 3.72 (2H, dd, J=14.2, 6.8 Hz), 3.47-3.38 (1H, m), 3.30-3.08 (3H, m), 2.79 (1H, sext, J=6.8 Hz), 1.35 (9H, s), 0.96 (3H, d, J=6.8 Hz).10256] MS: mlz=280 [M+H]
 

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