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Chemical Structure| 861892-40-2 Chemical Structure| 861892-40-2

Structure of 861892-40-2

Chemical Structure| 861892-40-2

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Product Details of [ 861892-40-2 ]

CAS No. :861892-40-2
Formula : C10H16O
M.W : 152.23
SMILES Code : CC(=C)[C@@H]1CCC(C)(O)C=C1
MDL No. :MFCD06797700

Safety of [ 861892-40-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P264-P280-P302+P352-P304+P340-P305+P351+P338

Application In Synthesis of [ 861892-40-2 ]

* 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 [ 861892-40-2 ]

[ 861892-40-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 56469-10-4 ]
  • [ 861892-40-2 ]
  • (6aR,10aR)-3-(1,1-Dimethyl-heptyl)-6,6,9-trimethyl-6a,7,10,10a-tetrahydro-6H-benzo[c]chromen-1-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
With toluene-4-sulfonic acid; In toluene; at 15 - 80℃; for 3h;Dean-Stark; To a 5-l, 3-neck round bottom flask was charged DMHR (240g, 1equiv), p-toluenesulfonic acid (40.8g, 0.2equiv) and toluene (1400ml). To this was added PMD (170g, 1.1equiv) over 1h, followed by a toluene (40ml) rinse while maintaining the batch temperature at 15-30C. The batch was heated to 70-80C under partial vacuum, and a Dean-Stark trap filled with toluene was used to remove water azeotropically while maintaining the same volume of toluene. The reaction was determined complete after 2h by HPLC, meeting the specification of 2.0% (AUC) compound 1. At atmospheric pressure, pyridine (13.4g, 1.6equiv) was added over ?15min while maintaining the batch temperature at 70-80C. Acetic anhydride (165.9g, 1.6equiv) was then added to the reactor over ?20min, again maintaining the batch temperature at 70-80C. After 2.5h the batch was sampled and passed the specification of compound 1 2.0% (AUC). Room temperature water (1920ml, 8equiv) was added and the batch was held at ambient temperature overnight. At ?25C, the phases were allowed to settle and the lower aqueous layer was removed. The batch was washed further with 480ml of room temperature water. A white emulsion was observed and a heat gun was required to produce a clean phase split. After the aqueous layer was removed, the reaction mixture was transferred to a 3-l, single-neck round bottom flask and placed on the rotary evaporator. The batch was concentrated down to ?600g (?1/3 of original reaction mixture) and isopropyl alcohol (IPA) (1.2L, 5equiv) was added. This was repeated 2 more times and then tested by NMR to determine the residual toluene level. The sample passed the specification of 2% toluene. The reaction mixture (1563g) was then split into several batches for crystallization experiments. Half of the reaction mixture (782g) was crystallized from an 8:2 IPA/water solution (240mL IPA and 240mL water was added to obtain the ratio). The batch temperature was adjusted to 45-55C. As it cooled down to 40-45C, crystals were observed. The batch was further cooled down to 20-25C at 10C/h and held overnight. Then, the batch was placed in an ice bath, filtered and washed with pre-chilled IPA/water (400ml, 4:1 IPA/water). The cake was pulled dry on the filter and then transferred to the vacuum oven where it was dried at 45-55C. The product was offloaded and gave compound 2 (147.32g, 70.3% yield).
With toluene-4-sulfonic acid; In toluene; at 15 - 80℃; for 2.63333h;Large scale; Step 1 To a 200-gallon reactor were charged ultrapure DMHR (20.0kg, 1 equiv.), PTSA (3.40kg, 0.2 equiv.) and toluene (102.3kg, 5 vol. equiv.). To this was added PMD (14.18kg, 1.1 equiv.) over 38 min, followed by a toluene rinse (17.4kg, 1 vol. equiv.) while maintaining the batch temperature at 15-30C. The batch was heated to 70-80C under partial vacuum, and a Dean-Stark trap filled with toluene was used to remove water by azeotropic distillation with toluene while maintaining a constant volume of toluene. The reaction was determined complete after 2h by HPLC, detecting no cannabidiol and obtaining a Delta8: Delta9 ratio of 106: 1 (specification was <2.0% (AUC) cannabidiol and Delta8: Delta9 ratio > 4: 1). The batch was held overnight at 25C and atmospheric pressure.
 

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