Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butyl nitrite | HCID 10996 | — |
| Reactant | methyl 2-(5-chlorobenzo[b]thiophen-3-yl)acetate | HCID 2779863 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Product | HCID 86739865 | HCID 86739865 | — |
Reaction Steps
Reaction of chloroacetone with 4-chlorothiophenol gave (4-chlorophenyl)thiomethyl methyl ketone, which was cyclized by reaction with polyphosphoric acid to 5-chloro-3-methylbenzothiophene. Bromination of the latter compound by photochemical reaction with N-bromosuccinimide provided 5-chloro-3-bromomethylbenzothiophene, which was reacted with sodium cyanide to give 5-chloro-3-cyanomethylbenzothiophene. The latter compound was hydrolyzed and esterified to give methyl α-(5-chloro-3-benzothienyl)acetate. Reaction of the ester with sodium methoxide and n-butyl nitrite afforded methyl α-hydroxyimino-α-(5-chloro-3-benzothienyl)acetate. Reduction of the oxime by reaction with zinc and formic acid and subsequent reaction with di-tert.-butyl carbonate gave N-tert.-butoxycarbonyl-(5-chloro-3-benzothienyl)glycine. NMR (CDCl3): δ 1.1-1.5 (broad s, 9H); δ 5.4-5.7 (broad s, 1H); δ 7.2-8.0 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04492693 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-2cd3271bbbce4df3b2849a1d73bfd008 |
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| Source note | uspto-grants-1985_01 |
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