JPS6254288B2 - - Google Patents
Info
- Publication number
- JPS6254288B2 JPS6254288B2 JP6972480A JP6972480A JPS6254288B2 JP S6254288 B2 JPS6254288 B2 JP S6254288B2 JP 6972480 A JP6972480 A JP 6972480A JP 6972480 A JP6972480 A JP 6972480A JP S6254288 B2 JPS6254288 B2 JP S6254288B2
- Authority
- JP
- Japan
- Prior art keywords
- cis
- grignard reagent
- general formula
- formula
- halo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000007818 Grignard reagent Substances 0.000 claims description 11
- 150000004795 grignard reagents Chemical class 0.000 claims description 11
- -1 copper halide Chemical class 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 125000006416 CBr Chemical group BrC* 0.000 claims 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 14
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- 239000000877 Sex Attractant Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000000543 intermediate Substances 0.000 description 5
- BXJHOKLLMOYSRQ-QOXWLJPHSA-N [(7z,11z)-hexadeca-7,11-dienyl] acetate Chemical compound CCCC\C=C/CC\C=C/CCCCCCOC(C)=O BXJHOKLLMOYSRQ-QOXWLJPHSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 229910021589 Copper(I) bromide Inorganic materials 0.000 description 3
- NKNDPYCGAZPOFS-UHFFFAOYSA-M copper(i) bromide Chemical compound Br[Cu] NKNDPYCGAZPOFS-UHFFFAOYSA-M 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- SUCYDSJQVVGOIW-WAYWQWQTSA-N 8Z-Dodecenyl acetate Chemical compound CCC\C=C/CCCCCCCOC(C)=O SUCYDSJQVVGOIW-WAYWQWQTSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 241000254173 Coleoptera Species 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 241000218691 Cupressaceae Species 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- XXPBOEBNDHAAQH-UHFFFAOYSA-N (Z)-12-Tetradecenyl acetate Natural products CCCCC=CCCCCCCCCOC(C)=O XXPBOEBNDHAAQH-UHFFFAOYSA-N 0.000 description 1
- BDOOYDRTBWAVQH-UHFFFAOYSA-N 1,6-dibromohex-1-yne Chemical compound BrCCCCC#CBr BDOOYDRTBWAVQH-UHFFFAOYSA-N 0.000 description 1
- SPNMFERZTLVHJE-UHFFFAOYSA-N 1,8-dibromooct-1-yne Chemical compound BrCCCCCCC#CBr SPNMFERZTLVHJE-UHFFFAOYSA-N 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- XXPBOEBNDHAAQH-SREVYHEPSA-N 9Z-Tetradecenyl acetate Chemical compound CCCC\C=C/CCCCCCCCOC(C)=O XXPBOEBNDHAAQH-SREVYHEPSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- 229910021595 Copper(I) iodide Inorganic materials 0.000 description 1
- 241000237858 Gastropoda Species 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 1
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 description 1
- 229940045803 cuprous chloride Drugs 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 230000026030 halogenation Effects 0.000 description 1
- 238000005658 halogenation reaction Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000011981 lindlar catalyst Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- ZKUUVVYMPUDTGJ-UHFFFAOYSA-N methyl 5-hydroxy-4-methoxy-2-nitrobenzoate Chemical compound COC(=O)C1=CC(O)=C(OC)C=C1[N+]([O-])=O ZKUUVVYMPUDTGJ-UHFFFAOYSA-N 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000011056 potassium acetate Nutrition 0.000 description 1
- ORQYPOUSZINNCB-UHFFFAOYSA-N potassium;hypobromite Chemical compound [K+].Br[O-] ORQYPOUSZINNCB-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6972480A JPS56166130A (en) | 1980-05-26 | 1980-05-26 | Preparation of alkynyl halide compound |
| DE8181103926T DE3165969D1 (en) | 1980-05-26 | 1981-05-21 | Alkynyl halide compounds and alkenyl acetate compounds therefrom |
| EP81103926A EP0040829B1 (en) | 1980-05-26 | 1981-05-21 | Alkynyl halide compounds and alkenyl acetate compounds therefrom |
| US06/266,614 US4391984A (en) | 1980-05-26 | 1981-05-22 | Alkynyl halide compounds and alkenyl acetate compounds therefrom |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6972480A JPS56166130A (en) | 1980-05-26 | 1980-05-26 | Preparation of alkynyl halide compound |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS56166130A JPS56166130A (en) | 1981-12-21 |
| JPS6254288B2 true JPS6254288B2 (zh) | 1987-11-13 |
Family
ID=13411065
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6972480A Granted JPS56166130A (en) | 1980-05-26 | 1980-05-26 | Preparation of alkynyl halide compound |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS56166130A (zh) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58128330A (ja) * | 1982-01-26 | 1983-07-30 | Shin Etsu Chem Co Ltd | ５−クロロ−１−ブロモ−１−ペンチン |
-
1980
- 1980-05-26 JP JP6972480A patent/JPS56166130A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS56166130A (en) | 1981-12-21 |
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