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Chemical Structure| 103733-65-9 Chemical Structure| 103733-65-9
Chemical Structure| 103733-65-9

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Synonyms: D-phenylalanine analogue

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Product Details of H-D-Tic-OH

CAS No. :103733-65-9
Formula : C10H11NO2
M.W : 177.20
SMILES Code : OC(=O)[C@H]1CC2=C(CN1)C=CC=C2
Synonyms :
D-phenylalanine analogue
MDL No. :MFCD00144038
InChI Key :BWKMGYQJPOAASG-SECBINFHSA-N
Pubchem ID :712398

Safety of H-D-Tic-OH

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of H-D-Tic-OH

* 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 [ 103733-65-9 ]

[ 103733-65-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 67-56-1 ]
  • [ 103733-65-9 ]
  • [ 146074-43-3 ]
YieldReaction ConditionsOperation in experiment
94.4% With thionyl chloride; at 0 - 20℃; for 100h; Compound 5 (4.27 g, 20 mmol) was added to 20 mL of methanol,After cooling to 0 C, 5.2 mL of thionyl chloride was added dropwise and the mixture was stirred at room temperature for 100 hours.Drying under reduced pressure, the residue was washed with ether,After drying, 4.3 g of light yellow solid compound 6 was obtained in a yield of 94.4%.
With thionyl chloride; at 0℃; for 2h;Inert atmosphere; Reflux; Thionyl chloride (210 μL, 3.12 mmol) was added dropwise to a solution of compound 10.1 (150 mg, 0.85 mmol) in methanol (5 mL) at 0 C. The reaction mixture was then refluxed for 2 h. The excess SOCl2 and methanol were then concentrated invacuo to get the crude compound 10.2 (132 mg). This compound was directly used in the next step without further purification.
  • 2
  • [ 103733-65-9 ]
  • [ 6624-49-3 ]
 

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