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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412415Generated: October 31, 2026

Butyl nitrite → HCID 86739865, compound

https://huagongshe.com/reaction/2412415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl nitriteHCID 10996—
Reactantmethyl 2-(5-chlorobenzo[b]thiophen-3-yl)acetateHCID 2779863—
ReactantSodium MethoxideHCID 10942334—
ProductHCID 86739865HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04492693
Source datasetuspto-grants-1985_01
ORD IDord-2cd3271bbbce4df3b2849a1d73bfd008
Source noteuspto-grants-1985_01