FR2244741A1 - Ether prepn. from lower alkanols and olefins - pref. methanol and isobutylene, using macro-crosslinked sulphonated ion exchange resin catalyst - Google Patents
Ether prepn. from lower alkanols and olefins - pref. methanol and isobutylene, using macro-crosslinked sulphonated ion exchange resin catalystInfo
- Publication number
- FR2244741A1 FR2244741A1 FR7427391A FR7427391A FR2244741A1 FR 2244741 A1 FR2244741 A1 FR 2244741A1 FR 7427391 A FR7427391 A FR 7427391A FR 7427391 A FR7427391 A FR 7427391A FR 2244741 A1 FR2244741 A1 FR 2244741A1
- Authority
- FR
- France
- Prior art keywords
- pref
- isobutylene
- ether
- contg
- prepn
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/05—Preparation of ethers by addition of compounds to unsaturated compounds
- C07C41/06—Preparation of ethers by addition of compounds to unsaturated compounds by addition of organic compounds only
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)
Abstract
Aliphatic ethers are prepd by contacting a charge contg a lower alkanol, (I) and =25 wt. % olefin, (II) in a (I):(II) mol ratio =1.5 at 26.7-93.8 (43.3-76.7 degrees C) pref. under 7-28.1 atmos, excess press. with a macro-crosslinked sulphonated ion exchange resin catalyst. In a pref. process a 4- or 3-4C petroleum raffinate stream contg. isobutylene as (II) is reacted with MeOH as (I) to form a prod contg. Me tert. Bu ether. The process is used for working up petroleum fractions contg. small amts of ios-olefins by in situ conversion of the olefines to ethers, and esp. prepn of Me tert. Bu ether which has a high octane no. and lower b. pt. than standard 8C alkylates prepd from isobutylene.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US40087373A | 1973-09-26 | 1973-09-26 |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2244741A1 true FR2244741A1 (en) | 1975-04-18 |
FR2244741B3 FR2244741B3 (en) | 1977-06-03 |
Family
ID=23585365
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR7427391A Granted FR2244741A1 (en) | 1973-09-26 | 1974-08-07 | Ether prepn. from lower alkanols and olefins - pref. methanol and isobutylene, using macro-crosslinked sulphonated ion exchange resin catalyst |
Country Status (5)
Country | Link |
---|---|
JP (1) | JPS5058006A (en) |
DE (1) | DE2445774A1 (en) |
FR (1) | FR2244741A1 (en) |
IT (1) | IT1022306B (en) |
NL (1) | NL7412620A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3264594B2 (en) * | 1994-01-27 | 2002-03-11 | キヤノン株式会社 | Recording device |
-
1974
- 1974-08-07 FR FR7427391A patent/FR2244741A1/en active Granted
- 1974-08-29 JP JP9845174A patent/JPS5058006A/ja active Pending
- 1974-09-24 NL NL7412620A patent/NL7412620A/en unknown
- 1974-09-25 DE DE19742445774 patent/DE2445774A1/en active Pending
- 1974-09-25 IT IT2769874A patent/IT1022306B/en active
Also Published As
Publication number | Publication date |
---|---|
FR2244741B3 (en) | 1977-06-03 |
IT1022306B (en) | 1978-03-20 |
NL7412620A (en) | 1975-04-01 |
DE2445774A1 (en) | 1975-04-03 |
JPS5058006A (en) | 1975-05-20 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
ST | Notification of lapse |