SU575023A3 - Method of preparing n-isopropyl-a-chloroacetanilide - Google Patents
Method of preparing n-isopropyl-a-chloroacetanilideInfo
- Publication number
- SU575023A3 SU575023A3 SU7301894271A SU1894271A SU575023A3 SU 575023 A3 SU575023 A3 SU 575023A3 SU 7301894271 A SU7301894271 A SU 7301894271A SU 1894271 A SU1894271 A SU 1894271A SU 575023 A3 SU575023 A3 SU 575023A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- isopropyl
- chloroacetanilide
- temperature
- preparing
- mol
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Description
lype в течение 2 ч кип т т с обратным холодильником . После этого реакционную смесь охлаждают. После охлаждени реакционную смесь смешивают с 600 мл воды, после чего образуютс две фазы. Верхн фаза содержит N - иэопрогаш - а -хлорацетанилкд, а нижн , водна фаза - гидрохлорид N,N - диизопрошшанилина. Из верхней фазы посредством промывкн водой удал ют загр знени кислотного характера.The lype is refluxed for 2 hours. After that, the reaction mixture is cooled. After cooling, the reaction mixture is mixed with 600 ml of water, after which two phases are formed. The upper phase contains N - isoprogash - a - chloroacetanilcd, and the lower, aqueous phase contains N, N hydrochloride - diisoproshaniline. Contaminants of an acidic nature are removed from the upper phase by washing with water.
После отгонки бензола получают 192г N тизопрошл - а хлорацетшшшща.After distillation of benzene, 192 g of N tisol is obtained — and chloroacetic acid.
Выход 90,9%. Степень шототы ,96%. Температура пл. 78-80° С.Yield 90.9%. The degree of shot, 96%. Temperature pl. 78-80 ° C.
Нюкшою водную фазу вейтршшзуют 40%-ным раствором едкого натра, после го высвобождайный N,N дкз зощ}О1шлашшш1 отдел ют, в спучш необходимости он может быть ушгчтозкен косредством сжигани .The aqueous phase is weighted with a 40% caustic soda solution, after the liberated N, N dkz zhosch} O1 slash 1 is separated, and if necessary, it can be disposed of by means of incineration.
П р и м е р 2. 135 г (1 мо ь) N - изопропиланшпша и 77 г (i мо ь) Ы,Н диизсшрохшлзнишша помещают в колбу, снабзкешгуш мешалкой, подвод щим штуцером, обрат1Ш1м холодальникшй и термометроь. При темаературе 40° С при вереьсешиканий и охлаждешш дс авд ют 100 г (1,05 моль) монохлоруксусной КИСЛОТЫ и 55 г (0,4 моль) PCEjC такой . скоростью, чтобы температура оставалась иа уровне 40° С. жремещеин в течение i ч смесь нагревают до кег вератури 110° С а реакционную в течеюш 2 ч вы}у1 к&вают при этой темнературе. Посш охлаждени до температуры 80° С реакщкнасую смесь смешивают сEXAMPLE 2. 135 g (1 mo) of N-isopropylenes and 77 g (i of) can be placed in a flask, equipped with a stirrer, choke, inverse, 1 × 1 m refrigerant and thermometer. With a temperature of 40 ° C with overlapping and cooling of ds, 100 g (1.05 mol) of monochloroacetic acid and 55 g (0.4 mol) of PCEjC are found. At a rate of 40 ° C, the temperature would remain at 40 ° C. The mixture will be heated to ip 110 ° C for i h for a reaction time and for 2 hours you will have a reaction time for this temperature. After cooling to a temperature of 80 ° C, the reaction mixture is mixed with
600 мл воды, N - изопропил - а - хлорацеташшид осаждают в виде масл нистой нижней фазы, а раствор N, N - диизопропиланилина образует верхнюю фазу.600 ml of water, N - isopropyl - a - chloroacetachid precipitate in the form of an oily lower phase, and the solution of N, N - diisopropylaniline forms the upper phase.
После разделени фаз нижнюю фазу раствор ют в бензоле, промьшают водой до нейтральной реакцщ и бензол отгон ют.After separation of the phases, the lower phase is dissolved in benzene, washed with water until neutral and the benzene is distilled off.
Получают 190 г N - изопропил - и - хлорацетанилида . Выход 90%. Температура пл. 78-80° С.190 g of N - isopropyl - and - chloroacetanilide are obtained. Yield 90%. Temperature pl. 78-80 ° C.
Примерз. Процесс провод т по примеру 2, исход из смеси 135 г (1 моль) N - изопропиланкшша и 88 г (0,5 моль) N,N - диизопропиланшшна и ре&кциош1ую смесь в течение 6 ч выдерЖЁшают при температуре 110° С.Froze The process is carried out as described in Example 2, starting from a mixture of 135 g (1 mol) of N - isopropyl anne and 88 g (0.5 mol) of N, N - diisopropylamine and a reagent mixture is aged for 6 hours at a temperature of 110 ° C.
Выход и степень чистого продукта соответствуют значени л указ иным в примере 2,The yield and degree of pure product correspond to the value of decree different in example 2
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU72NI00000151A HU171936B (en) | 1972-08-28 | 1972-08-28 | Process for producing pure n-izopropyl-alpha -chloroacetanilide |
Publications (1)
Publication Number | Publication Date |
---|---|
SU575023A3 true SU575023A3 (en) | 1977-09-30 |
Family
ID=10999988
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU7301894271A SU575023A3 (en) | 1972-08-28 | 1973-03-14 | Method of preparing n-isopropyl-a-chloroacetanilide |
Country Status (8)
Country | Link |
---|---|
BG (1) | BG26807A3 (en) |
DE (1) | DE2304615C3 (en) |
ES (1) | ES411613A1 (en) |
HU (1) | HU171936B (en) |
IT (1) | IT988604B (en) |
RO (1) | RO63834A (en) |
SU (1) | SU575023A3 (en) |
YU (1) | YU39601B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115490608A (en) * | 2022-10-19 | 2022-12-20 | 阿拉善盟锦源科技发展有限公司 | Production method of propachlor |
-
1972
- 1972-08-28 HU HU72NI00000151A patent/HU171936B/en not_active IP Right Cessation
-
1973
- 1973-01-26 BG BG2253573A patent/BG26807A3/xx unknown
- 1973-01-30 RO RO7366073A patent/RO63834A/en unknown
- 1973-01-31 DE DE19732304615 patent/DE2304615C3/en not_active Expired
- 1973-02-14 ES ES411613A patent/ES411613A1/en not_active Expired
- 1973-03-02 IT IT2114373A patent/IT988604B/en active
- 1973-03-14 SU SU7301894271A patent/SU575023A3/en active
- 1973-03-20 YU YU75573A patent/YU39601B/en unknown
Also Published As
Publication number | Publication date |
---|---|
DE2304615C3 (en) | 1981-10-22 |
YU75573A (en) | 1982-02-28 |
DE2304615A1 (en) | 1974-03-21 |
ES411613A1 (en) | 1976-05-16 |
IT988604B (en) | 1975-04-30 |
HU171936B (en) | 1978-04-28 |
DE2304615B2 (en) | 1980-12-04 |
YU39601B (en) | 1985-03-20 |
BG26807A3 (en) | 1979-06-12 |
RO63834A (en) | 1978-12-15 |
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